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Human Disease Vocabulary Browser
The current vocabulary contains human disease, syndrome, and condition terms from Online Mendelian Inheritance in Man (OMIM database).
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Human Diseases/Syndromes Beginning with "M"

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OMIM IDHuman Disease
OMIM:247990 MacDermot-Winter Syndrome
OMIM:109150 Machado-Joseph Disease; MJD
OMIM:618286 Macrocephaly, Acquired, with Impaired Intellectual Development; MACID
OMIM:606369 Macrocephaly and Epileptic Encephalopathy
OMIM:605309 Macrocephaly/Autism Syndrome
OMIM:153470 Macrocephaly, Benign Familial
OMIM:617011 Macrocephaly, Dysmorphic Facies, and Psychomotor Retardation; MDFPMR
OMIM:248000 Macrocephaly/Megalencephaly Syndrome, Autosomal Recessive; MGCPH
OMIM:619769 Macrocephaly, Neurodevelopmental Delay, Lymphoid Hyperplasia, and Persistent Fetal Hemoglobin; MNDLFH
OMIM:600084 Macrocytosis, Familial
OMIM:155500 Macrodactyly
OMIM:248010 Macroepiphyseal Dysplasia with Osteoporosis, Wrinkled Skin, and Aged Appearance
OMIM:153600 Macroglobulinemia, Waldenstrom, Susceptibility to, 1; WM1
OMIM:610430 Macroglobulinemia, Waldenstrom, Susceptibility to, 2; WM2
OMIM:153630 Macroglossia
OMIM:602499 Macrophthalmia, Colobomatous, with Microcornea; MACOM
OMIM:248100 Macrosomia Adiposa Congenita
OMIM:248110 Macrosomia with Microphthalmia, Lethal
OMIM:613545 Macrostomia, Isolated
OMIM:155100 Macrothrombocytopenia and Granulocyte Inclusions with or without Nephritis or Sensorineural Hearing Loss; MATINS
OMIM:613112 Macrothrombocytopenia, Isolated, 1, Autosomal Dominant; MACTHC1
OMIM:619840 Macrothrombocytopenia, Isolated, 2, Autosomal Dominant; MACTHC2
OMIM:613075 Macs Syndrome
OMIM:611488 Macular Degeneration, Age-Related, 10; ARMD10
OMIM:611953 Macular Degeneration, Age-Related, 11; ARMD11
OMIM:613784 Macular Degeneration, Age-Related, 12; ARMD12
OMIM:615439 Macular Degeneration, Age-Related, 13; ARMD13
OMIM:615489 Macular Degeneration, Age-Related, 14; ARMD14
OMIM:615591 Macular Degeneration, Age-Related, 15; ARMD15
OMIM:603075 Macular Degeneration, Age-Related, 1; ARMD1
OMIM:153800 Macular Degeneration, Age-Related, 2; ARMD2
OMIM:608895 Macular Degeneration, Age-Related, 3; ARMD3
OMIM:610698 Macular Degeneration, Age-Related, 4; ARMD4
OMIM:613761 Macular Degeneration, Age-Related, 5; ARMD5
OMIM:613757 Macular Degeneration, Age-Related, 6; ARMD6
OMIM:610149 Macular Degeneration, Age-Related, 7; ARMD7
OMIM:613778 Macular Degeneration, Age-Related, 8; ARMD8
OMIM:611378 Macular Degeneration, Age-Related, 9; ARMD9
OMIM:300834 Macular Degeneration, Atrophic, X-Linked
OMIM:616118 Macular Degeneration, Early-Onset; EOMD
OMIM:217800 Macular Dystrophy, Corneal; MCD
OMIM:153880 Macular Dystrophy, Dominant Cystoid; DCMD
OMIM:153890 Macular Dystrophy, Fenestrated Sheen Type
OMIM:169150 Macular Dystrophy, Patterned, 1; MDPT1
OMIM:608970 Macular Dystrophy, Patterned, 2; MDPT2
OMIM:617111 Macular Dystrophy, Patterned, 3; MDPT3
OMIM:136550 Macular Dystrophy, Retinal, 1, North Carolina Type; MCDR1
OMIM:608051 Macular Dystrophy, Retinal, 2; MCDR2
OMIM:608850 Macular Dystrophy, Retinal, 3; MCDR3
OMIM:619977 Macular Dystrophy, Retinal, 4; MCDR4
OMIM:153840 Macular Dystrophy, Vitelliform, 1; VMD1
OMIM:153700 Macular Dystrophy, Vitelliform, 2; VMD2
OMIM:608161 Macular Dystrophy, Vitelliform, 3; VMD3
OMIM:616151 Macular Dystrophy, Vitelliform, 4; VMD4
OMIM:616152 Macular Dystrophy, Vitelliform, 5; VMD5
OMIM:616170 Macular Dystrophy with Central Cone Involvement; CCMD
OMIM:620762 Macular Dystrophy with or without Cone Dysfunction; MDCD
OMIM:309100 Macular Dystrophy, X-Linked
OMIM:248260 Magnesium, Elevated Red Cell
OMIM:619290 Mahvash Disease; MVAH
OMIM:609628 Majeed Syndrome; MJDS
OMIM:125480 Major Affective Disorder 1; MAFD1
OMIM:309200 Major Affective Disorder 2; MAFD2
OMIM:609633 Major Affective Disorder 3; MAFD3
OMIM:611247 Major Affective Disorder 4; MAFD4
OMIM:611535 Major Affective Disorder 5; MAFD5
OMIM:611536 Major Affective Disorder 6; MAFD6
OMIM:612371 Major Affective Disorder 7; MAFD7
OMIM:612357 Major Affective Disorder 8; MAFD8
OMIM:612372 Major Affective Disorder 9; MAFD9
OMIM:608520 Major Depressive Disorder 1
OMIM:608691 Major Depressive Disorder 2
OMIM:608516 Major Depressive Disorder; MDD
OMIM:142830 Major Histocompatibility Complex, Class I, B; HLA-B
OMIM:614753 Malan Syndrome; MALNS
OMIM:609148 Malaria, Mild, Susceptibility to
OMIM:611162 Malaria, Susceptibility to
OMIM:248300 Mal De Meleda; MDM
OMIM:617596 Maleylacetoacetate Isomerase Deficiency; MAAID
OMIM:602248 Malignant Atrophic Papulosis
OMIM:145600 Malignant Hyperthermia, Susceptibility to, 1; MHS1
OMIM:154275 Malignant Hyperthermia, Susceptibility to, 2
OMIM:154276 Malignant Hyperthermia, Susceptibility to, 3
OMIM:600467 Malignant Hyperthermia, Susceptibility to, 4
OMIM:601887 Malignant Hyperthermia, Susceptibility to, 5; MHS5
OMIM:601888 Malignant Hyperthermia, Susceptibility to, 6
OMIM:248350 Malocclusion and Short Stature
OMIM:154300 Malocclusion Due to Protuberant Upper Front Teeth
OMIM:248360 Malonyl-CoA Decarboxylase Deficiency
OMIM:189490 Malposition of Teeth with or without Hypodontia/Oligodontia
OMIM:613689 Mammary-Digital-Nail Syndrome; MDNS
OMIM:154370 Mammastatin
OMIM:607308 Mammographic Density
OMIM:615381 Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome; MDPL
OMIM:619127 Mandibuloacral Dysplasia Progeroid Syndrome; MDPS
OMIM:248370 Mandibuloacral Dysplasia with Type A Lipodystrophy; MADA
OMIM:608612 Mandibuloacral Dysplasia with Type B Lipodystrophy; MADB
OMIM:610536 Mandibulofacial Dysostosis, Guion-Almeida Type; MFDGA
OMIM:604830 Mandibulofacial Dysostosis Syndrome, Bauru Type
OMIM:616367 Mandibulofacial Dysostosis with Alopecia; MFDA
OMIM:248400 Mandibulofacial Dysostosis with Impaired Intellectual Development
OMIM:602562 Mandibulofacial Dysostosis with Macroblepharon and Macrostomia
OMIM:608257 Mandibulofacial Dysostosis with Ptosis, Autosomal Dominant
OMIM:248450 Manitoba Oculotrichoanal Syndrome; MOTA
OMIM:154570 Mannose 6-Phosphate Receptor Recognition Defect, Lebanese Type
OMIM:614372 Mannose-Binding Lectin Deficiency; MBLD
OMIM:248500 Mannosidosis, Alpha B, Lysosomal; MANSA
OMIM:248510 Mannosidosis, Beta A, Lysosomal; MANSB
OMIM:615135 Maple Syrup Urine Disease, Mild Variant; MSUDMV
OMIM:248600 Maple Syrup Urine Disease, Type IA; MSUD1A
OMIM:620698 Maple Syrup Urine Disease, Type IB; MSUD1B
OMIM:620699 Maple Syrup Urine Disease, Type II; MSUD2
OMIM:619322 Marbach-Rustad Progeroid Syndrome; MARUPS
OMIM:619680 Marbach-Schaaf Neurodevelopmental Syndrome; MASNS
OMIM:154600 Marcus Gunn Phenomenon
OMIM:248700 Marden-Walker Syndrome; MWKS
OMIM:248760 Marfanoid Habitus with Microcephaly and Glomerulonephritis
OMIM:609008 Marfanoid Habitus with Situs Inversus
OMIM:154750 Marfanoid Hypermobility Syndrome
OMIM:248770 Marfanoid Impaired Intellectual Developmental Syndrome, Autosomal
OMIM:616914 Marfanoid-Progeroid-Lipodystrophy Syndrome; MFLS
OMIM:154700 Marfan Syndrome; MFS
OMIM:248800 Marinesco-Sjogren Syndrome; MSS
OMIM:602535 Marshall-Smith Syndrome; MRSHSS
OMIM:154780 Marshall Syndrome; MRSHS
OMIM:147430 Marsili Syndrome; MARSIS
OMIM:601346 Martinez-Frias Syndrome
OMIM:300519 Martin-Probst Syndrome; MRXSMP
OMIM:212720 Martsolf Syndrome 1; MARTS1
OMIM:619420 Martsolf Syndrome 2; MARTS2
OMIM:303350 MASA Syndrome
OMIM:613791 Masp2 Deficiency
OMIM:604308 MASS Syndrome
OMIM:154850 Masticatory Muscles, Hypertrophy of
OMIM:154800 Mastocytosis, Cutaneous; MASTC
OMIM:248900 Mast Syndrome; MASTS
OMIM:606391 Maturity-Onset Diabetes of the Young; MODY
OMIM:613370 Maturity-Onset Diabetes of the Young, Type 10; MODY10
OMIM:613375 Maturity-Onset Diabetes of the Young, Type 11; MODY11
OMIM:616329 Maturity-Onset Diabetes of the Young, Type 13; MODY13
OMIM:616511 Maturity-Onset Diabetes of the Young, Type 14; MODY14
OMIM:125850 Maturity-Onset Diabetes of the Young, Type 1; MODY1
OMIM:125851 Maturity-Onset Diabetes of the Young, Type 2; MODY2
OMIM:600496 Maturity-Onset Diabetes of the Young, Type 3; MODY3
OMIM:606392 Maturity-Onset Diabetes of the Young, Type 4; MODY4
OMIM:606394 Maturity-Onset Diabetes of the Young, Type 6; MODY6
OMIM:610508 Maturity-Onset Diabetes of the Young, Type 7; MODY7
OMIM:609812 Maturity-Onset Diabetes of the Young, Type 8, with Exocrine Dysfunction; MODY8
OMIM:612225 Maturity-Onset Diabetes of the Young, Type 9; MODY9
OMIM:155000 Maxillofacial Dysostosis
OMIM:155050 Maxillonasal Dysplasia, Binder Type
OMIM:277000 Mayer-Rokitansky-Kuster-Hauser Syndrome; MRKH
OMIM:174800 McCune-Albright Syndrome; MAS
OMIM:248950 McDonough Syndrome
OMIM:236700 McKusick-Kaufman Syndrome; MKKS
OMIM:300842 Mcleod Syndrome; MCLDS
OMIM:608978 Meacham Syndrome
OMIM:155140 Meckel Diverticulum
OMIM:616258 Meckel Syndrome 12; MKS12
OMIM:617562 Meckel Syndrome 13; MKS13
OMIM:619879 Meckel Syndrome 14; MKS14
OMIM:614175 Meckel Syndrome, Type 10; MKS10
OMIM:615397 Meckel Syndrome, Type 11; MKS11
OMIM:249000 Meckel Syndrome, Type 1; MKS1
OMIM:603194 Meckel Syndrome, Type 2; MKS2
OMIM:607361 Meckel Syndrome, Type 3; MKS3
OMIM:611134 Meckel Syndrome, Type 4; MKS4
OMIM:611561 Meckel Syndrome, Type 5; MKS5
OMIM:612284 Meckel Syndrome, Type 6; MKS6
OMIM:267010 Meckel Syndrome, Type 7; MKS7
OMIM:613885 Meckel Syndrome, Type 8; MKS8
OMIM:614209 Meckel Syndrome, Type 9; MKS9
OMIM:614665 Meconium Ileus
OMIM:155200 Mediosternal Depigmentation Line
OMIM:602199 Medium Chain 3-Ketoacyl-CoA Thiolase Deficiency
OMIM:609313 Mednik Syndrome; MEDNIK
OMIM:155255 Medulloblastoma; MDB
OMIM:300989 Meester-Loeys Syndrome; MRLS
OMIM:618719 Megabladder, Congenital; MGBL
OMIM:618273 Mega-Corpus-Callosum Syndrome with Cerebellar Hypoplasia and Cortical Malformations; MCCCHCM
OMIM:249210 Megacystis-Microcolon-Intestinal Hypoperistalsis Syndrome 1; MMIHS1
OMIM:619351 Megacystis-Microcolon-Intestinal Hypoperistalsis Syndrome 2; MMIHS2
OMIM:619362 Megacystis-Microcolon-Intestinal Hypoperistalsis Syndrome 3; MMIHS3
OMIM:619365 Megacystis-Microcolon-Intestinal Hypoperistalsis Syndrome 4; MMIHS4
OMIM:619431 Megacystis-Microcolon-Intestinal Hypoperistalsis Syndrome 5; MMIHS5
OMIM:249230 Megaepiphyseal Dwarfism
OMIM:604004 Megalencephalic Leukoencephalopathy with Subcortical Cysts 1; MLC1
OMIM:613925 Megalencephalic Leukoencephalopathy with Subcortical Cysts 2A; MLC2A
OMIM:613926 Megalencephalic Leukoencephalopathy with Subcortical Cysts 2b, Remitting, with or without Impaired Intellectual Development; MLC2B
OMIM:620447 Megalencephalic Leukoencephalopathy with Subcortical Cysts 3; MLC3
OMIM:620448 Megalencephalic Leukoencephalopathy with Subcortical Cysts 4, Remitting; MLC4
OMIM:155350 Megalencephaly, Autosomal Dominant
OMIM:602501 Megalencephaly-Capillary Malformation-Polymicrogyria Syndrome; MCAP
OMIM:620748 Megalencephaly-Polydactyly Syndrome; MPAPA
OMIM:603387 Megalencephaly-Polymicrogyria-Polydactyly-Hydrocephalus Syndrome 1;
OMIM:615937 Megalencephaly-Polymicrogyria-Polydactyly-Hydrocephalus Syndrome 2;
OMIM:615938 Megalencephaly-Polymicrogyria-Polydactyly-Hydrocephalus Syndrome 3;
OMIM:249240 Megalencephaly with Dysmyelination
OMIM:613839 Megaloblastic Anemia Due to Dihydrofolate Reductase Deficiency
OMIM:601775 Megaloblastic Anemia, Folate-Responsive; MEGAF
OMIM:249300 Megalocornea
OMIM:309300 Megalocornea; MGC1
OMIM:612785 Megarbane-Jalkh Syndrome
OMIM:606527 Megarbane Syndrome
OMIM:300148 Mehmo Syndrome; MEHMO
OMIM:224690 Meier-Gorlin Syndrome 1; MGORS1
OMIM:613800 Meier-Gorlin Syndrome 2; MGORS2
OMIM:613803 Meier-Gorlin Syndrome 3; MGORS3
OMIM:613804 Meier-Gorlin Syndrome 4; MGORS4
OMIM:613805 Meier-Gorlin Syndrome 5; MGORS5
OMIM:616835 Meier-Gorlin Syndrome 6; MGORS6
OMIM:617063 Meier-Gorlin Syndrome 7; MGORS7
OMIM:617564 Meier-Gorlin Syndrome 8; MGORS8
OMIM:137550 Melanocytic Nevus Syndrome, Congenital; CMNS
OMIM:155755 Melanoma-Astrocytoma Syndrome
OMIM:155600 Melanoma, Cutaneous Malignant, Susceptibility to, 1; CMM1
OMIM:155601 Melanoma, Cutaneous Malignant, Susceptibility to, 2; CMM2
OMIM:609048 Melanoma, Cutaneous Malignant, Susceptibility to, 3; CMM3
OMIM:608035 Melanoma, Cutaneous Malignant, Susceptibility to, 4; CMM4
OMIM:613099 Melanoma, Cutaneous Malignant, Susceptibility to, 5; CMM5
OMIM:613972 Melanoma, Cutaneous Malignant, Susceptibility to, 6; CMM6
OMIM:612263 Melanoma, Cutaneous Malignant, Susceptibility to, 7; CMM7
OMIM:614456 Melanoma, Cutaneous Malignant, Susceptibility to, 8; CMM8
OMIM:615134 Melanoma, Cutaneous Malignant, Susceptibility to, 9; CMM9
OMIM:155700 Melanoma, Malignant Familial Intraocular
OMIM:606719 Melanoma-Pancreatic Cancer Syndrome
OMIM:155770 Melanoma Tumor Antigen Gp90
OMIM:155720 Melanoma, Uveal
OMIM:606660 Melanoma, Uveal, Susceptibility to, 1; UVM1
OMIM:606661 Melanoma, Uveal, Susceptibility to, 2; UVM2
OMIM:249400 Melanosis, Neurocutaneous; NCMS
OMIM:615557 Melioidosis, Susceptibility to
OMIM:155900 Melkersson-Rosenthal Syndrome
OMIM:309350 Melnick-Needles Syndrome; MNS
OMIM:155950 Melorheostosis, Isolated; MEL
OMIM:305800 Membranoproliferative Glomerulonephritis, X-Linked
OMIM:155980 Membranous Cranial Ossification, Delayed
OMIM:614692 Membranous Nephropathy, Susceptibility To; MBNP
OMIM:300960 Mend Syndrome; MEND
OMIM:156000 Meniere Disease
OMIM:607174 Meningioma, Familial, Susceptibility to
OMIM:606190 Meningioma, Radiation-Induced
OMIM:618332 Menke-Hennekam Syndrome 1; MKHK1
OMIM:618333 Menke-Hennekam Syndrome 2; MKHK2
OMIM:309400 Menkes Disease; MNK
OMIM:156190 Mental and Growth Retardation with Amblyopia
OMIM:309640 Mental Retardation with Spastic Paraplegia
OMIM:156220 Meralgia Paraesthetica, Familial
OMIM:249650 Mercaptolactate-Cysteine Disulfiduria; MCDU
OMIM:249670 Mesoaxial Hexadactyly and Cardiac Malformation
OMIM:600383 Mesomelia-Synostoses Syndrome
OMIM:156230 Mesomelic Dwarfism of Hypoplastic Tibia and Radius Type
OMIM:611886 Mesomelic Dysplasia, Camera Type
OMIM:156232 Mesomelic Dysplasia, Kantaputra Type; MMDK
OMIM:605274 Mesomelic Dysplasia, Savarirayan Type
OMIM:249710 Mesomelic Limb Shortening and Bowing
OMIM:156240 Mesothelioma, Malignant; MESOM
OMIM:616878 Metabolic Crises, Recurrent, with Rhabdomyolysis, Cardiac Arrhythmias, and Neurodegeneration; MECRCN
OMIM:618416 Metabolic Crises, Recurrent, with Variable Encephalomyopathic Features and Neurologic Regression; MECREN
OMIM:309630 Metacarpal 4-5 Fusion; MF4
OMIM:156250 Metachondromatosis; METCDS
OMIM:156300 Metachromasia of Fibroblasts
OMIM:156310 Metachromatic Leukodystrophy, Adult-Onset, with Normal Arylsulfatase A
OMIM:249900 Metachromatic Leukodystrophy Due to Saposin B Deficiency; MLDSAPB
OMIM:250100 Metachromatic Leukodystrophy; MLD
OMIM:250215 Metaphyseal Acroscyphodysplasia
OMIM:613073 Metaphyseal Anadysplasia 2; MANDP2
OMIM:156400 Metaphyseal Chondrodysplasia, Jansen Type; MCDJ
OMIM:250230 Metaphyseal Chondrodysplasia, Kaitila Type
OMIM:250300 Metaphyseal Chondrodysplasia, Pena Type
OMIM:156500 Metaphyseal Chondrodysplasia, Schmid Type; MCDS
OMIM:609989 Metaphyseal Chondrodysplasia with Cone-Shaped Epiphyses, Normal Hair, and Normal Hands
OMIM:250420 Metaphyseal Dysostosis, Impaired Intellectual Development, and Conductive Deafness
OMIM:250450 Metaphyseal Dysplasia, Anetoderma, and Optic Atrophy
OMIM:605946 Metaphyseal Dysplasia, Braun-Tinschert Type
OMIM:250400 Metaphyseal Dysplasia, Spahr Type; MDST
OMIM:156510 Metaphyseal Dysplasia with Maxillary Hypoplasia with or without Brachydactyly; MDMHB
OMIM:250460 Metaphyseal Dysplasia without Hypotrichosis; MDWH
OMIM:614875 Metaphyseal Enchondromatosis with D-2-Hydroxyglutaric Aciduria
OMIM:250500 Metaphyseal Modeling Abnormality, Skin Lesions, and Spastic Paraplegia
OMIM:608811 Metaphyseal Undermodeling, Spondylar Dysplasia, and Overgrowth
OMIM:156520 Metatarsus Varus, Type I
OMIM:156530 Metatropic Dysplasia; MTD
OMIM:617973 Methemoglobinemia, Alpha Type
OMIM:250790 Methemoglobinemia and Ambiguous Genitalia; METAG
OMIM:617971 Methemoglobinemia, Beta Type
OMIM:250800 Methemoglobinemia Due to Deficiency of Methemoglobin Reductase
OMIM:250700 Methemoglobin Reductase Deficiency
OMIM:250850 Methionine Adenosyltransferase I/Iii Deficiency
OMIM:250900 Methionine Malabsorption Syndrome
OMIM:614105 Methylmalonate Semialdehyde Dehydrogenase Deficiency; MMSDHD
OMIM:277400 Methylmalonic Aciduria and Homocystinuria, Cblc Type; MAHCC
OMIM:277410 Methylmalonic Aciduria and Homocystinuria, Cbld Type; MAHCD
OMIM:277380 Methylmalonic Aciduria and Homocystinuria, Cblf Type; MAHCF
OMIM:614857 Methylmalonic Aciduria and Homocystinuria, Cblj Type; MAHCJ
OMIM:620940 Methylmalonic Aciduria and Homocystinuria, Cbll Type; MAHCL
OMIM:309541 Methylmalonic Aciduria and Homocystinuria, Cblx Type; MAHCX
OMIM:251100 Methylmalonic Aciduria, Cbla Type; MACA
OMIM:251110 Methylmalonic Aciduria, Cblb Type; MACB
OMIM:620953 Methylmalonic Aciduria, Cbld Type; MACD
OMIM:251000 Methylmalonic Aciduria Due to Methylmalonyl-Coa Mutase Deficiency;
OMIM:613646 Methylmalonic Aciduria, Transient, Due to Transcobalamin Receptor Defect; MATR
OMIM:251120 Methylmalonyl-Coa Epimerase Deficiency
OMIM:610377 Mevalonic Aciduria; MEVA
OMIM:604571 Mhc Class I Deficiency 1; MHC1D1
OMIM:620813 Mhc Class I Deficiency 2; MHC1D2
OMIM:620814 Mhc Class I Deficiency 3; MHC1D3
OMIM:209920 Mhc Class II Deficiency 1; MHC2D1
OMIM:620815 Mhc Class II Deficiency 2; MHC2D2
OMIM:620816 Mhc Class II Deficiency 3; MHC2D3
OMIM:620817 Mhc Class II Deficiency 4; MHC2D4
OMIM:620818 Mhc Class II Deficiency 5; MHC2D5
OMIM:618564 Microangiopathy and Leukoencephalopathy, Pontine, Autosomal Dominant;
OMIM:210720 Microcephalic Osteodysplastic Primordial Dwarfism, Type II; MOPD2
OMIM:210710 Microcephalic Osteodysplastic Primordial Dwarfism, Type I; MOPD1
OMIM:210700 Microcephalic Primordial Dwarfism, Montreal Type
OMIM:251190 Microcephalic Primordial Dwarfism, Toriello Type
OMIM:615095 Microcephaly 10, Primary, Autosomal Recessive; MCPH10
OMIM:615414 Microcephaly 11, Primary, Autosomal Recessive; MCPH11
OMIM:616080 Microcephaly 12, Primary, Autosomal Recessive; MCPH12
OMIM:616051 Microcephaly 13, Primary, Autosomal Recessive; MCPH13
OMIM:616402 Microcephaly 14, Primary, Autosomal Recessive; MCPH14
OMIM:616681 Microcephaly 16, Primary, Autosomal Recessive; MCPH16
OMIM:617090 Microcephaly 17, Primary, Autosomal Recessive; MCPH17
OMIM:617520 Microcephaly 18, Primary, Autosomal Dominant; MCPH18
OMIM:617800 Microcephaly 19, Primary, Autosomal Recessive; MCPH19
OMIM:251200 Microcephaly 1, Primary, Autosomal Recessive; MCPH1
OMIM:617914 Microcephaly 20, Primary, Autosomal Recessive; MCPH20
OMIM:617983 Microcephaly 21, Primary, Autosomal Recessive; MCPH21
OMIM:617984 Microcephaly 22, Primary, Autosomal Recessive; MCPH22
OMIM:617985 Microcephaly 23, Primary, Autosomal Recessive; MCPH23
OMIM:618179 Microcephaly 24, Primary, Autosomal Recessive; MCPH24
OMIM:618351 Microcephaly 25, Primary, Autosomal Recessive; MCPH25
OMIM:619179 Microcephaly 26, Primary, Autosomal Dominant; MCPH26
OMIM:619180 Microcephaly 27, Primary, Autosomal Dominant; MCPH27
OMIM:619453 Microcephaly 28, Primary, Autosomal Recessive; MCPH28
OMIM:620047 Microcephaly 29, Primary, Autosomal Recessive; MCPH29
OMIM:604317 Microcephaly 2, Primary, Autosomal Recessive, with or without Cortical Malformations; MCPH2
OMIM:620183 Microcephaly 30, Primary, Autosomal Recessive; MCPH30
OMIM:604804 Microcephaly 3, Primary, Autosomal Recessive; MCPH3
OMIM:604321 Microcephaly 4, Primary, Autosomal Recessive; MCPH4
OMIM:608716 Microcephaly 5, Primary, Autosomal Recessive; MCPH5
OMIM:608393 Microcephaly 6, Primary, Autosomal Recessive; MCPH6
OMIM:612703 Microcephaly 7, Primary, Autosomal Recessive; MCPH7
OMIM:614673 Microcephaly 8, Primary, Autosomal Recessive; MCPH8
OMIM:614852 Microcephaly 9, Primary, Autosomal Recessive; MCPH9
OMIM:607196 Microcephaly, Amish Type; MCPHA
OMIM:251270 Microcephaly and Chorioretinopathy, Autosomal Recessive, 1; MCCRP1
OMIM:616171 Microcephaly and Chorioretinopathy, Autosomal Recessive, 2; MCCRP2
OMIM:616335 Microcephaly and Chorioretinopathy, Autosomal Recessive, 3; MCCRP3
OMIM:156580 Microcephaly, Autosomal Dominant
OMIM:614261 Microcephaly-Capillary Malformation Syndrome; MICCAP
OMIM:251220 Microcephaly-Cardiomyopathy
OMIM:618284 Microcephaly, Cataracts, Impaired Intellectual Development, and Dystonia with Abnormal Striatum; MCIDDS
OMIM:614407 Microcephaly, Cerebellar Hypoplasia, and Cardiac Conduction Defect Syndrome; MCHCCD
OMIM:616834 Microcephaly, Congenital Cataract, and Psoriasiform Dermatitis; MCCPD
OMIM:601355 Microcephaly, Congenital Heart Disease, Unilateral Renal Agenesis, and Hyposegmented Lungs
OMIM:601420 Microcephaly, Corpus Callosum Dysgenesis, and Cleft Lip/Palate
OMIM:156620 Microcephaly-Deafness Syndrome
OMIM:618891 Microcephaly, Developmental Delay, and Brittle Hair Syndrome; MDBH
OMIM:614231 Microcephaly, Epilepsy, and Diabetes Syndrome 1; MEDS1
OMIM:619278 Microcephaly, Epilepsy, and Diabetes Syndrome 2; MEDS2
OMIM:603572 Microcephaly, Facial Abnormalities, Micromelia, and Impaired Intellectual Development
OMIM:618142 Microcephaly, Facial Dysmorphism, Renal Agenesis, and Ambiguous Genitalia Syndrome; MFRG
OMIM:618346 Microcephaly, Growth Deficiency, Seizures, and Brain Malformations;
OMIM:618097 Microcephaly, Growth Restriction, and Increased Sister Chromatid Exchange 2; MGRISCE2
OMIM:612947 Microcephaly, Growth Retardation, Cataract, Hearing Loss, and Unusual Appearance
OMIM:602555 Microcephaly, Macrotia, and Impaired Intellectual Development
OMIM:251230 Microcephaly-Micromelia Syndrome; MIMIS
OMIM:613668 Microcephaly, Postnatal Progressive, with Seizures and Brain Atrophy
OMIM:615760 Microcephaly, Progressive, with Seizures and Cerebral and Cerebellar Atrophy; MSCCA
OMIM:601537 Microcephaly, Retinitis Pigmentosa, and Sutural Cataract
OMIM:613402 Microcephaly, Seizures, and Developmental Delay; MCSZ
OMIM:603394 Microcephaly, Severe, with Skeletal Anomalies Including Posterior Rib-Gap Defects
OMIM:616033 Microcephaly, Short Stature, and Impaired Glucose Metabolism 1;
OMIM:616817 Microcephaly, Short Stature, and Impaired Glucose Metabolism 2;
OMIM:617604 Microcephaly, Short Stature, and Limb Abnormalities; MISSLA
OMIM:614833 Microcephaly, Short Stature, and Polymicrogyria with or without Seizures; MSSP
OMIM:251250 Microcephaly with Cervical Spine Fusion Anomalies
OMIM:251240 Microcephaly with Chemotactic Defect and Transient Hypogammaglobulinemia
OMIM:152950 Microcephaly with or without Chorioretinopathy, Lymphedema, or Impaired Intellectual Development; MCLMR
OMIM:603802 Microcephaly with Simplified Gyral Pattern
OMIM:251400 Microcolon
OMIM:156600 Microcoria, Congenital
OMIM:156700 Microcornea, Glaucoma, and Absent Frontal Sinuses
OMIM:615458 Microcornea, Myopic Chorioretinal Atrophy, and Telecanthus; MMCAT
OMIM:619082 Microcornea, Rod-Cone Dystrophy, Cataract, and Posterior Staphyloma 1; MRCS1
OMIM:156810 Microgastria-Limb Reduction Defects Association; MLRD
OMIM:605013 Microhydranencephaly; MHAC
OMIM:306990 Microhydranencephaly, X-Linked; MHACX
OMIM:156830 Micromelic Bone Dysplasia with Cloverleaf Skull
OMIM:616428 Microphthalmia/Coloboma 10; MCOPCB10
OMIM:620731 Microphthalmia/Coloboma 11; MCOPCB11
OMIM:120200 Microphthalmia/Coloboma 12; MCOPCB12
OMIM:620968 Microphthalmia/Coloboma 13; MCOPCB13
OMIM:300345 Microphthalmia/Coloboma 1; MCOPCB1
OMIM:605738 Microphthalmia/Coloboma 2; MCOPCB2
OMIM:610092 Microphthalmia/Coloboma 3; MCOPCB3
OMIM:251505 Microphthalmia/Coloboma 4; MCOPCB4
OMIM:611638 Microphthalmia/Coloboma 5; MCOPCB5
OMIM:613703 Microphthalmia/Coloboma 6; MCOPCB6
OMIM:614497 Microphthalmia/Coloboma 7; MCOPCB7
OMIM:615145 Microphthalmia/Coloboma 9; MCOPCB9
OMIM:615877 Microphthalmia/Coloboma and Skeletal Dysplasia Syndrome; MCSKS
OMIM:251600 Microphthalmia, Isolated 1; MCOP1
OMIM:610093 Microphthalmia, Isolated 2; MCOP2
OMIM:613094 Microphthalmia, Isolated 4; MCOP4
OMIM:611040 Microphthalmia, Isolated 5; MCOP5
OMIM:613517 Microphthalmia, Isolated 6; MCOP6
OMIM:613704 Microphthalmia, Isolated 7; MCOP7
OMIM:615113 Microphthalmia, Isolated 8; MCOP8
OMIM:156850 Microphthalmia, Isolated, with Cataract 1; MCOPCT1
OMIM:156900 Microphthalmia, Isolated, with Corectopia; MCOPCR
OMIM:611222 Microphthalmia, Syndromic 10; MCOPS10
OMIM:614402 Microphthalmia, Syndromic 11; MCOPS11
OMIM:615524 Microphthalmia, Syndromic 12; MCOPS12
OMIM:300915 Microphthalmia, Syndromic 13; MCOPS13
OMIM:611038 Microphthalmia, Syndromic 16; MCOPS16
OMIM:309800 Microphthalmia, Syndromic 1; MCOPS1
OMIM:300166 Microphthalmia, Syndromic 2; MCOPS2
OMIM:206900 Microphthalmia, Syndromic 3; MCOPS3
OMIM:610125 Microphthalmia, Syndromic 5; MCOPS5
OMIM:607932 Microphthalmia, Syndromic 6; MCOPS6
OMIM:601349 Microphthalmia, Syndromic 8; MCOPS8
OMIM:601186 Microphthalmia, Syndromic 9; MCOPS9
OMIM:607597 Microphthalmia with Cyst, Bilateral Facial Clefts, and Limb Anomalies
OMIM:251700 Microphthalmia with Hyperopia, Retinal Degeneration, Macrophakia, and Dental Anomalies
OMIM:206920 Microphthalmia with Limb Anomalies; MLA
OMIM:251750 Microspherophakia and/or Megalocornea, with Ectopia Lentis and with or without Secondary Glaucoma; MSPKA
OMIM:157151 Microspherophakia-Metaphyseal Dysplasia
OMIM:157150 Microspherophakia with Hernia
OMIM:600674 Microtia-Anotia
OMIM:612290 Microtia, Hearing Impairment, and Cleft Palate
OMIM:251800 Microtia with Meatal Atresia and Conductive Deafness
OMIM:611863 Microtia with Nasolacrimal Duct Imperforation and Eye Coloboma
OMIM:603933 Microvascular Complications of Diabetes, Susceptibility to, 1; MVCD1
OMIM:612623 Microvascular Complications of Diabetes, Susceptibility to, 2; MVCD2
OMIM:612624 Microvascular Complications of Diabetes, Susceptibility to, 3; MVCD3
OMIM:612628 Microvascular Complications of Diabetes, Susceptibility to, 4; MVCD4
OMIM:612633 Microvascular Complications of Diabetes, Susceptibility to, 5; MVCD5
OMIM:612634 Microvascular Complications of Diabetes, Susceptibility to, 6; MVCD6
OMIM:612635 Microvascular Complications of Diabetes, Susceptibility to, 7; MVCD7
OMIM:300990 Midface Hypoplasia, Hearing Impairment, Elliptocytosis, and Nephrocalcinosis; MFHIEN
OMIM:608624 Midface Hypoplasia, Obesity, Developmental Delay, and Neonatal Hypotonia
OMIM:601016 Midline Malformations, Multiple, with Limb Abnormalities and Hypopituitarism
OMIM:249600 Mietens-Weber Syndrome
OMIM:141500 Migraine, Familial Hemiplegic, 1; FHM1
OMIM:602481 Migraine, Familial Hemiplegic, 2; FHM2
OMIM:609634 Migraine, Familial Hemiplegic, 3; FHM3
OMIM:613656 Migraine with Aura, Susceptibility to, 13; MGR13
OMIM:609179 Migraine with Aura, Susceptibility to, 7
OMIM:609670 Migraine with Aura, Susceptibility to, 9
OMIM:157300 Migraine with or without Aura, Susceptibility to, 1
OMIM:610208 Migraine with or without Aura, Susceptibility to, 10
OMIM:610209 Migraine with or without Aura, Susceptibility to, 11
OMIM:611706 Migraine with or without Aura, Susceptibility to, 12; MGR12
OMIM:300125 Migraine with or without Aura, Susceptibility to, 2
OMIM:607498 Migraine with or without Aura, Susceptibility to, 3
OMIM:607508 Migraine with or without Aura, Susceptibility to, 5
OMIM:607516 Migraine with or without Aura, Susceptibility to, 6
OMIM:609570 Migraine with or without Aura, Susceptibility to, 8
OMIM:607501 Migraine without Aura, Susceptibility to, 4
OMIM:157400 Milia, Multiple Eruptive; MEM
OMIM:247200 Miller-Dieker Lissencephaly Syndrome; MDLS
OMIM:263750 Miller Syndrome
OMIM:157570 Minisatellite 33.15
OMIM:157560 Minisatellite 33.6
OMIM:617053 Mirage Syndrome; MIRAGE
OMIM:268050 Mirhosseini-Holmes-Walton Syndrome
OMIM:157600 Mirror Movements 1; MRMV1
OMIM:614508 Mirror Movements 2; MRMV2
OMIM:616059 Mirror Movements 3; MRMV3
OMIM:618264 Mirror Movements 4; MRMV4
OMIM:276300 Mismatch Repair Cancer Syndrome 1; MMRCS1
OMIM:619096 Mismatch Repair Cancer Syndrome 2; MMRCS2
OMIM:619097 Mismatch Repair Cancer Syndrome 3; MMRCS3
OMIM:619101 Mismatch Repair Cancer Syndrome 4; MMRCS4
OMIM:615710 Mitchell-Riley Syndrome; MTCHRS
OMIM:618960 Mitchell Syndrome; MITCH
OMIM:500014 Mitochondrial Complex I Deficiency, Mitochondrial Type 1; MC1DM1
OMIM:618233 Mitochondrial Complex I Deficiency, Nuclear Type 10; MC1DN10
OMIM:618234 Mitochondrial Complex I Deficiency, Nuclear Type 11; MC1DN11
OMIM:301020 Mitochondrial Complex I Deficiency, Nuclear Type 12; MC1DN12
OMIM:618235 Mitochondrial Complex I Deficiency, Nuclear Type 13; MC1DN13
OMIM:618236 Mitochondrial Complex I Deficiency, Nuclear Type 14; MC1DN14
OMIM:618237 Mitochondrial Complex I Deficiency, Nuclear Type 15; MC1DN15
OMIM:618238 Mitochondrial Complex I Deficiency, Nuclear Type 16; MC1DN16
OMIM:618239 Mitochondrial Complex I Deficiency, Nuclear Type 17; MC1DN17
OMIM:618240 Mitochondrial Complex I Deficiency, Nuclear Type 18; MC1DN18
OMIM:618241 Mitochondrial Complex I Deficiency, Nuclear Type 19; MC1DN19
OMIM:252010 Mitochondrial Complex I Deficiency, Nuclear Type 1; MC1DN1
OMIM:611126 Mitochondrial Complex I Deficiency, Nuclear Type 20; MC1DN20
OMIM:618242 Mitochondrial Complex I Deficiency, Nuclear Type 21; MC1DN21
OMIM:618243 Mitochondrial Complex I Deficiency, Nuclear Type 22; MC1DN22
OMIM:618244 Mitochondrial Complex I Deficiency, Nuclear Type 23; MC1DN23
OMIM:618245 Mitochondrial Complex I Deficiency, Nuclear Type 24; MC1DN24
OMIM:618246 Mitochondrial Complex I Deficiency, Nuclear Type 25; MC1DN25
OMIM:618247 Mitochondrial Complex I Deficiency, Nuclear Type 26; MC1DN26
OMIM:618248 Mitochondrial Complex I Deficiency, Nuclear Type 27; MC1DN27
OMIM:618249 Mitochondrial Complex I Deficiency, Nuclear Type 28; MC1DN28
OMIM:618250 Mitochondrial Complex I Deficiency, Nuclear Type 29; MC1DN29
OMIM:618222 Mitochondrial Complex I Deficiency, Nuclear Type 2; MC1DN2
OMIM:301021 Mitochondrial Complex I Deficiency, Nuclear Type 30; MC1DN30
OMIM:618251 Mitochondrial Complex I Deficiency, Nuclear Type 31; MC1DN31
OMIM:618252 Mitochondrial Complex I Deficiency, Nuclear Type 32; MC1DN32
OMIM:618253 Mitochondrial Complex I Deficiency, Nuclear Type 33; MC1DN33
OMIM:618776 Mitochondrial Complex I Deficiency, Nuclear Type 34; MC1DN34
OMIM:619003 Mitochondrial Complex I Deficiency, Nuclear Type 35; MC1DN35
OMIM:619170 Mitochondrial Complex I Deficiency, Nuclear Type 36; MC1DN36
OMIM:619272 Mitochondrial Complex I Deficiency, Nuclear Type 37; MC1DN37
OMIM:620135 Mitochondrial Complex I Deficiency, Nuclear Type 39; MC1DN39
OMIM:618224 Mitochondrial Complex I Deficiency, Nuclear Type 3; MC1DN3
OMIM:618225 Mitochondrial Complex I Deficiency, Nuclear Type 4; MC1DN4
OMIM:618226 Mitochondrial Complex I Deficiency, Nuclear Type 5; MC1DN5
OMIM:618228 Mitochondrial Complex I Deficiency, Nuclear Type 6; MC1DN6
OMIM:618229 Mitochondrial Complex I Deficiency, Nuclear Type 7; MC1DN7
OMIM:618230 Mitochondrial Complex I Deficiency, Nuclear Type 8; MC1DN8
OMIM:618232 Mitochondrial Complex I Deficiency, Nuclear Type 9; MC1DN9
OMIM:252011 Mitochondrial Complex II Deficiency, Nuclear Type 1; MC2DN1
OMIM:619166 Mitochondrial Complex II Deficiency, Nuclear Type 2; MC2DN2
OMIM:619167 Mitochondrial Complex II Deficiency, Nuclear Type 3; MC2DN3
OMIM:619224 Mitochondrial Complex II Deficiency, Nuclear Type 4; MC2DN4
OMIM:618775 Mitochondrial Complex III Deficiency, Nuclear Type 10; MC3DN10
OMIM:620137 Mitochondrial Complex III Deficiency, Nuclear Type 11; MC3DN11
OMIM:124000 Mitochondrial Complex III Deficiency, Nuclear Type 1; MC3DN1
OMIM:615157 Mitochondrial Complex III Deficiency, Nuclear Type 2; MC3DN2
OMIM:615158 Mitochondrial Complex III Deficiency, Nuclear Type 3; MC3DN3
OMIM:615159 Mitochondrial Complex III Deficiency, Nuclear Type 4; MC3DN4
OMIM:615160 Mitochondrial Complex III Deficiency, Nuclear Type 5; MC3DN5
OMIM:615453 Mitochondrial Complex III Deficiency, Nuclear Type 6; MC3DN6
OMIM:615824 Mitochondrial Complex III Deficiency, Nuclear Type 7; MC3DN7
OMIM:615838 Mitochondrial Complex III Deficiency, Nuclear Type 8; MC3DN8
OMIM:616111 Mitochondrial Complex III Deficiency, Nuclear Type 9; MC3DN9
OMIM:619053 Mitochondrial Complex IV Deficiency, Nuclear Type 10; MC4DN10
OMIM:619054 Mitochondrial Complex IV Deficiency, Nuclear Type 11; MC4DN11
OMIM:619055 Mitochondrial Complex IV Deficiency, Nuclear Type 12; MC4DN12
OMIM:616501 Mitochondrial Complex IV Deficiency, Nuclear Type 13; MC4DN13
OMIM:619058 Mitochondrial Complex IV Deficiency, Nuclear Type 14; MC4DN14
OMIM:619059 Mitochondrial Complex IV Deficiency, Nuclear Type 15; MC4DN15
OMIM:619060 Mitochondrial Complex IV Deficiency, Nuclear Type 16; MC4DN16
OMIM:619061 Mitochondrial Complex IV Deficiency, Nuclear Type 17; MC4DN17
OMIM:619062 Mitochondrial Complex IV Deficiency, Nuclear Type 18; MC4DN18
OMIM:619063 Mitochondrial Complex IV Deficiency, Nuclear Type 19; MC4DN19
OMIM:220110 Mitochondrial Complex IV Deficiency, Nuclear Type 1; MC4DN1
OMIM:619064 Mitochondrial Complex IV Deficiency, Nuclear Type 20; MC4DN20
OMIM:619065 Mitochondrial Complex IV Deficiency, Nuclear Type 21; MC4DN21
OMIM:619355 Mitochondrial Complex IV Deficiency, Nuclear Type 22; MC4DN22
OMIM:620275 Mitochondrial Complex IV Deficiency, Nuclear Type 23; MC4DN23
OMIM:604377 Mitochondrial Complex IV Deficiency, Nuclear Type 2; MC4DN2
OMIM:619046 Mitochondrial Complex IV Deficiency, Nuclear Type 3; MC4DN3
OMIM:619048 Mitochondrial Complex IV Deficiency, Nuclear Type 4; MC4DN4
OMIM:220111 Mitochondrial Complex IV Deficiency, Nuclear Type 5; MC4DN5
OMIM:615119 Mitochondrial Complex IV Deficiency, Nuclear Type 6; MC4DN6
OMIM:619051 Mitochondrial Complex IV Deficiency, Nuclear Type 7; MC4DN7
OMIM:619052 Mitochondrial Complex IV Deficiency, Nuclear Type 8; MC4DN8
OMIM:616500 Mitochondrial Complex IV Deficiency, Nuclear Type 9; MC4DN9
OMIM:500015 Mitochondrial Complex V (atp Synthase) Deficiency, Mitochondrial Type 1; MC5DM1
OMIM:604273 Mitochondrial Complex V (atp Synthase) Deficiency, Nuclear Type 1;
OMIM:614052 Mitochondrial Complex V (atp Synthase) Deficiency, Nuclear Type 2;
OMIM:614053 Mitochondrial Complex V (atp Synthase) Deficiency, Nuclear Type 3;
OMIM:620358 Mitochondrial Complex V (atp Synthase) Deficiency, Nuclear Type 4A;
OMIM:615228 Mitochondrial Complex V (atp Synthase) Deficiency, Nuclear Type 4b;
OMIM:618120 Mitochondrial Complex V (atp Synthase) Deficiency, Nuclear Type 5;
OMIM:618683 Mitochondrial Complex V (atp Synthase) Deficiency, Nuclear Type 6;
OMIM:620359 Mitochondrial Complex V (atp Synthase) Deficiency, Nuclear Type 7;
OMIM:615084 Mitochondrial DNA Depletion Syndrome 11; MTDPS11
OMIM:617184 Mitochondrial DNA Depletion Syndrome 12a (cardiomyopathic Type), Autosomal Dominant; MTDPS12A
OMIM:615418 Mitochondrial DNA Depletion Syndrome 12b (cardiomyopathic Type), Autosomal Recessive; MTDPS12B
OMIM:615471 Mitochondrial DNA Depletion Syndrome 13 (encephalomyopathic Type);
OMIM:616896 Mitochondrial DNA Depletion Syndrome 14 (cardioencephalomyopathic Type); MTDPS14
OMIM:617156 Mitochondrial DNA Depletion Syndrome 15 (hepatocerebral Type);
OMIM:619425 Mitochondrial DNA Depletion Syndrome 16b (neuroophthalmic Type);
OMIM:618528 Mitochondrial DNA Depletion Syndrome 16 (hepatic Type); MTDPS16
OMIM:618567 Mitochondrial DNA Depletion Syndrome 17; MTDPS17
OMIM:618811 Mitochondrial DNA Depletion Syndrome 18; MTDPS18
OMIM:618972 Mitochondrial DNA Depletion Syndrome 19; MTDPS19
OMIM:603041 Mitochondrial DNA Depletion Syndrome 1 (mngie Type); MTDPS1
OMIM:619780 Mitochondrial DNA Depletion Syndrome 20 (mngie Type); MTDPS20
OMIM:609560 Mitochondrial DNA Depletion Syndrome 2 (myopathic Type); MTDPS2
OMIM:251880 Mitochondrial DNA Depletion Syndrome 3 (hepatocerebral Type); MTDPS3
OMIM:203700 Mitochondrial DNA Depletion Syndrome 4a (alpers Type); MTDPS4A
OMIM:613662 Mitochondrial DNA Depletion Syndrome 4b (mngie Type); MTDPS4B
OMIM:612073 Mitochondrial DNA Depletion Syndrome 5 (encephalomyopathic with or without Methylmalonic Aciduria); MTDPS5
OMIM:256810 Mitochondrial DNA Depletion Syndrome 6 (hepatocerebral Type); MTDPS6
OMIM:271245 Mitochondrial DNA Depletion Syndrome 7 (hepatocerebral Type); MTDPS7
OMIM:612075 Mitochondrial DNA Depletion Syndrome 8a (encephalomyopathic Type with Renal Tubulopathy); MTDPS8A
OMIM:245400 Mitochondrial DNA Depletion Syndrome 9 (encephalomyopathic Type with Methylmalonic Aciduria); MTDPS9
OMIM:600851 Mitochondrial Import-Stimulating Factor
OMIM:602252 Mitochondrial Intermembrane Space Protein Tim12, Yeast, Homolog of
OMIM:540000 Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-Like Episodes; MELAS
OMIM:251900 Mitochondrial Myopathy, Episodic, with or without Optic Atrophy and Reversible Leukoencephalopathy; MEOAL
OMIM:500009 Mitochondrial Myopathy, Infantile, Transient; MMIT
OMIM:551000 Mitochondrial Myopathy, Lethal, Infantile; LIMM
OMIM:251945 Mitochondrial Myopathy with A Defect in Mitochondrial-Protein Transport
OMIM:500002 Mitochondrial Myopathy with Diabetes
OMIM:251950 Mitochondrial Myopathy with Lactic Acidosis; MMLA
OMIM:610773 Mitochondrial Phosphate Carrier Deficiency; MPCD
OMIM:614741 Mitochondrial Pyruvate Carrier Deficiency; MPYCD
OMIM:616277 Mitochondrial Short-Chain Enoyl-Coa Hydratase 1 Deficiency; ECHS1D
OMIM:609015 Mitochondrial Trifunctional Protein Deficiency 1; MTPD1
OMIM:620300 Mitochondrial Trifunctional Protein Deficiency 2; MTPD2
OMIM:157700 Mitral Valve Prolapse 1; MVP1
OMIM:607829 Mitral Valve Prolapse 2; MVP2
OMIM:610840 Mitral Valve Prolapse 3; MVP3
OMIM:254130 Miyoshi Muscular Dystrophy 1; MMD1
OMIM:613318 Miyoshi Muscular Dystrophy 2; MMD2
OMIM:613319 Miyoshi Muscular Dystrophy 3; MMD3
OMIM:309840 Modifier, X-Linked, for Neurofunctional Defects
OMIM:157900 Moebius Syndrome; MBS
OMIM:304700 Mohr-Tranebjaerg Syndrome; MTS
OMIM:223540 Mollica Syndrome
OMIM:252150 Molybdenum Cofactor Deficiency, Type A; MOCODA
OMIM:252160 Molybdenum Cofactor Deficiency, Type B; MOCODB
OMIM:615501 Molybdenum Cofactor Deficiency, Type C; MOCODC
OMIM:157980 MOMO Syndrome
OMIM:158000 Monilethrix; MNLIX
OMIM:616095 Monocarboxylate Transporter 1 Deficiency; MCT1D
OMIM:252250 Monocyte Chemotactic Disorder
OMIM:613353 Mononeuropathy of the Median Nerve, Mild; MNMN
OMIM:158100 Monophalangy of Great Toe
OMIM:231630 Monosodium Glutamate Sensitivity
OMIM:252270 Monosomy 7 Myelodysplasia and Leukemia Syndrome 1; M7MLS1
OMIM:619041 Monosomy 7 Myelodysplasia and Leukemia Syndrome 2; M7MLS2
OMIM:615703 Morbid Obesity and Spermatogenic Failure; MOSPGF
OMIM:252300 Morquio Syndrome C
OMIM:257300 Mosaic Variegated Aneuploidy Syndrome 1; MVA1
OMIM:614114 Mosaic Variegated Aneuploidy Syndrome 2; MVA2
OMIM:617598 Mosaic Variegated Aneuploidy Syndrome 3; MVA3
OMIM:620153 Mosaic Variegated Aneuploidy Syndrome 4; MVA4
OMIM:620189 Mosaic Variegated Aneuploidy Syndrome 7 with Inflammation and Tumor Predisposition; MVA7
OMIM:158280 Motion Sickness
OMIM:600333 Motor Neuron Disease with Dementia and Ophthalmoplegia
OMIM:252320 Motor Neuropathy, Peripheral, with Dysautonomia
OMIM:235730 Mowat-Wilson Syndrome; MOWS
OMIM:252350 Moyamoya Disease 1; MYMY1
OMIM:607151 Moyamoya Disease 2; MYMY2
OMIM:608796 Moyamoya Disease 3; MYMY3
OMIM:300845 Moyamoya Disease 4 with Short Stature, Hypergonadotropic Hypogonadism, and Facial Dysmorphism; MYMY4
OMIM:614042 Moyamoya Disease 5; MYMY5
OMIM:615750 Moyamoya Disease 6 with or without Achalasia; MYMY6
OMIM:620687 Moyamoya Disease 7; MYMY7
OMIM:613342 Mseleni Joint Disease
OMIM:191900 Muckle-Wells Syndrome; MWS
OMIM:158310 Mucoepithelial Dysplasia, Hereditary; HMD
OMIM:252500 Mucolipidosis II Alpha/Beta
OMIM:252600 Mucolipidosis III Alpha/Beta
OMIM:252605 Mucolipidosis III Gamma
OMIM:252650 Mucolipidosis IV; ML4
OMIM:617303 Mucopolysaccharidosis-Plus Syndrome; MPSPS
OMIM:252900 Mucopolysaccharidosis, Type IIIA; MPS3A
OMIM:252920 Mucopolysaccharidosis, Type IIIB; MPS3B
OMIM:252930 Mucopolysaccharidosis, Type Iiic; MPS3C
OMIM:252940 Mucopolysaccharidosis, Type Iiid; MPS3D
OMIM:309900 Mucopolysaccharidosis, Type II; MPS2
OMIM:253000 Mucopolysaccharidosis, Type IVA; MPS4A
OMIM:253010 Mucopolysaccharidosis, Type Ivb; MPS4B
OMIM:601492 Mucopolysaccharidosis, Type IX; MPS9
OMIM:253220 Mucopolysaccharidosis, Type VII; MPS7
OMIM:253200 Mucopolysaccharidosis, Type VI; MPS6
OMIM:619698 Mucopolysaccharidosis, Type X; MPS10
OMIM:253240 Mucus Inspissation of Respiratory Tract
OMIM:602849 Muenke Syndrome; MNKES
OMIM:158320 Muir-Torre Syndrome; MRTES
OMIM:617352 Mulchandani-Bhoj-Conlin Syndrome; MBCS
OMIM:253250 Mulibrey Nanism; MUL
OMIM:301022 Mullegama-Klein-Martinez Syndrome; MKMS
OMIM:158330 Mullerian Aplasia and Hyperandrogenism
OMIM:235255 Mullerian Derivatives, Persistence of, with Lymphangiectasia and Postaxial Polydactyly
OMIM:601076 Mullerian Duct Aplasia, Unilateral Renal Agenesis, and Cervicothoracic Somite Anomalies; MURCS
OMIM:166300 Multicentric Carpotarsal Osteolysis Syndrome; MCTO
OMIM:259600 Multicentric Osteolysis, Nodulosis, and Arthropathy; MONA
OMIM:236500 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly; MARCH
OMIM:231680 Multiple Acyl-CoA Dehydrogenase Deficiency; MADD
OMIM:614080 Multiple Congenital Anomalies-Hypotonia-Seizures Syndrome 1; MCAHS1
OMIM:300868 Multiple Congenital Anomalies-Hypotonia-Seizures Syndrome 2; MCAHS2
OMIM:615398 Multiple Congenital Anomalies-Hypotonia-Seizures Syndrome 3; MCAHS3
OMIM:618548 Multiple Congenital Anomalies-Hypotonia-Seizures Syndrome 4; MCAHS4
OMIM:301056 Multiple Congenital Anomalies-Neurodevelopmental Syndrome, X-Linked;
OMIM:607161 Multiple Congenital Anomalies Syndrome with Cloverleaf Skull
OMIM:614569 Multiple Enchondromatosis, Maffucci Type
OMIM:171400 Multiple Endocrine Neoplasia, Type IIA; MEN2A
OMIM:162300 Multiple Endocrine Neoplasia, Type IIB; MEN2B
OMIM:131100 Multiple Endocrine Neoplasia, Type I; MEN1
OMIM:610755 Multiple Endocrine Neoplasia, Type IV; MEN4
OMIM:601560 Multiple Epiphyseal Dysplasia with Robin Phenotype
OMIM:158345 Multiple Exostoses with Spastic Tetraparesis
OMIM:615554 Multiple Fibroadenomas of the Breast; MFAB
OMIM:245600 Multiple Joint Dislocations, Short Stature, and Craniofacial Dysmorphism with or without Congenital Heart Defects; JDSCD
OMIM:620960 Multiple Mitochondrial Dysfunctions Syndrome 10; MMDS10
OMIM:605711 Multiple Mitochondrial Dysfunctions Syndrome 1; MMDS1
OMIM:614299 Multiple Mitochondrial Dysfunctions Syndrome 2 with Hyperglycinemia;
OMIM:615330 Multiple Mitochondrial Dysfunctions Syndrome 3; MMDS3
OMIM:616370 Multiple Mitochondrial Dysfunctions Syndrome 4; MMDS4
OMIM:617613 Multiple Mitochondrial Dysfunctions Syndrome 5; MMDS5
OMIM:617954 Multiple Mitochondrial Dysfunctions Syndrome 6; MMDS6
OMIM:620423 Multiple Mitochondrial Dysfunctions Syndrome 7; MMDS7
OMIM:620887 Multiple Mitochondrial Dysfunctions Syndrome 9b; MMDS9B
OMIM:265000 Multiple Pterygium Syndrome, Escobar Variant; EVMPS
OMIM:253290 Multiple Pterygium Syndrome, Lethal Type; LMPS
OMIM:312150 Multiple Pterygium Syndrome, X-Linked
OMIM:612594 Multiple Sclerosis, Susceptibility to, 2; MS2
OMIM:612595 Multiple Sclerosis, Susceptibility to, 3; MS3
OMIM:612596 Multiple Sclerosis, Susceptibility to, 4; MS4
OMIM:614810 Multiple Sclerosis, Susceptibility to, 5; MS5
OMIM:126200 Multiple Sclerosis, Susceptibility To; MS
OMIM:132800 Multiple Self-Healing Squamous Epithelioma, Susceptibility To; MSSE
OMIM:272200 Multiple Sulfatase Deficiency; MSD
OMIM:186500 Multiple Synostoses Syndrome 1; SYNS1
OMIM:610017 Multiple Synostoses Syndrome 2; SYNS2
OMIM:612961 Multiple Synostoses Syndrome 3; SYNS3
OMIM:617898 Multiple Synostoses Syndrome 4; SYNS4
OMIM:146500 Multiple System Atrophy 1, Susceptibility To; MSA1
OMIM:611376 Mungan Syndrome; MGS
OMIM:158400 Muscle Cramps, Familial
OMIM:614160 Muscle Hypertrophy; MSLHP
OMIM:158500 Muscular Atrophy, Ataxia, Retinitis Pigmentosa, and Diabetes Mellitus
OMIM:158650 Muscular Atrophy, Malignant Neurogenic
OMIM:253590 Muscular Dystrophy, Adult-Onset, with Leukoencephalopathy
OMIM:616827 Muscular Dystrophy, Autosomal Recessive, with Cardiomyopathy and Triangular Tongue; MDRCMTT
OMIM:158800 Muscular Dystrophy, Barnes Type
OMIM:300376 Muscular Dystrophy, Becker Type; BMD
OMIM:309930 Muscular Dystrophy, Cardiac Type
OMIM:604801 Muscular Dystrophy, Congenital, 1B; MDC1B
OMIM:617066 Muscular Dystrophy, Congenital, Davignon-Chauveau Type; MDCDC
OMIM:613204 Muscular Dystrophy, Congenital, Due to Integrin Alpha-7 Deficiency
OMIM:619518 Muscular Dystrophy, Congenital Hearing Loss, and Ovarian Insufficiency Syndrome; MDHLO
OMIM:613205 Muscular Dystrophy, Congenital, Lmna-Related
OMIM:602541 Muscular Dystrophy, Congenital, Megaconial Type; MDCMC
OMIM:607855 Muscular Dystrophy, Congenital Merosin-Deficient, 1A; MDC1A
OMIM:617404 Muscular Dystrophy, Congenital, with Cataracts and Impaired Intellectual Development; MDCCAID
OMIM:603323 Muscular Dystrophy, Congenital, with Cerebellar Atrophy
OMIM:254000 Muscular Dystrophy, Congenital, with Infantile Cataract and Hypogonadism
OMIM:620166 Muscular Dystrophy, Congenital, with or without Seizures; MYOS
OMIM:254100 Muscular Dystrophy, Congenital, with Rapid Progression; MDRP
OMIM:601170 Muscular Dystrophy, Congenital, with Severe Central Nervous System Atrophy and Absence of Large Myelinated Fibers
OMIM:310200 Muscular Dystrophy, Duchenne Type; DMD
OMIM:615041 Muscular Dystrophy-Dystroglycanopathy (congenital with Brain and Eye Anomalies), Type A, 10; MDDGA10
OMIM:615181 Muscular Dystrophy-Dystroglycanopathy (congenital with Brain and Eye Anomalies), Type A, 11; MDDGA11
OMIM:615249 Muscular Dystrophy-Dystroglycanopathy (congenital with Brain and Eye Anomalies), Type A, 12; MDDGA12
OMIM:615287 Muscular Dystrophy-Dystroglycanopathy (congenital with Brain and Eye Anomalies), Type A, 13; MDDGA13
OMIM:615350 Muscular Dystrophy-Dystroglycanopathy (congenital with Brain and Eye Anomalies), Type A, 14; MDDGA14
OMIM:236670 Muscular Dystrophy-Dystroglycanopathy (congenital with Brain and Eye Anomalies), Type A, 1; MDDGA1
OMIM:613150 Muscular Dystrophy-Dystroglycanopathy (congenital with Brain and Eye Anomalies), Type A, 2; MDDGA2
OMIM:253280 Muscular Dystrophy-Dystroglycanopathy (congenital with Brain and Eye Anomalies), Type A, 3; MDDGA3
OMIM:253800 Muscular Dystrophy-Dystroglycanopathy (congenital with Brain and Eye Anomalies), Type A, 4; MDDGA4
OMIM:613153 Muscular Dystrophy-Dystroglycanopathy (congenital with Brain and Eye Anomalies), Type A, 5; MDDGA5
OMIM:613154 Muscular Dystrophy-Dystroglycanopathy (congenital with Brain and Eye Anomalies), Type A, 6; MDDGA6
OMIM:614643 Muscular Dystrophy-Dystroglycanopathy (congenital with Brain and Eye Anomalies), Type A, 7; MDDGA7
OMIM:614830 Muscular Dystrophy-Dystroglycanopathy (congenital with Brain and Eye Anomalies), Type A, 8; MDDGA8
OMIM:616538 Muscular Dystrophy-Dystroglycanopathy (congenital with Brain and Eye Anomalies), Type A, 9; MDDGA9
OMIM:615351 Muscular Dystrophy-Dystroglycanopathy (congenital with Impaired Intellectual Development), Type B, 14; MDDGB14
OMIM:618992 Muscular Dystrophy-Dystroglycanopathy (congenital with Impaired Intellectual Development), Type B, 15; MDDGB15
OMIM:613155 Muscular Dystrophy-Dystroglycanopathy (congenital with Impaired Intellectual Development), Type B, 1; MDDGB1
OMIM:613156 Muscular Dystrophy-Dystroglycanopathy (congenital with Impaired Intellectual Development), Type B, 2; MDDGB2
OMIM:613151 Muscular Dystrophy-Dystroglycanopathy (congenital with Impaired Intellectual Development), Type B, 3; MDDGB3
OMIM:608840 Muscular Dystrophy-Dystroglycanopathy (congenital with Impaired Intellectual Development), Type B, 6; MDDGB6
OMIM:606612 Muscular Dystrophy-Dystroglycanopathy (congenital with or without Impaired Intellectual Development), Type B, 5; MDDGB5
OMIM:613152 Muscular Dystrophy-Dystroglycanopathy (congenital without Impaired Intellectual Development), Type B, 4; MDDGB4
OMIM:609308 Muscular Dystrophy-Dystroglycanopathy (limb-Girdle), Type C, 1;
OMIM:616094 Muscular Dystrophy-Dystroglycanopathy (limb-Girdle), Type C, 12;
OMIM:615352 Muscular Dystrophy-Dystroglycanopathy (limb-Girdle), Type C, 14;
OMIM:612937 Muscular Dystrophy-Dystroglycanopathy (limb-Girdle), Type C, 15;
OMIM:613158 Muscular Dystrophy-Dystroglycanopathy (limb-Girdle), Type C, 2;
OMIM:613157 Muscular Dystrophy-Dystroglycanopathy (limb-Girdle), Type C, 3;
OMIM:611588 Muscular Dystrophy-Dystroglycanopathy (limb-Girdle), Type C, 4;
OMIM:607155 Muscular Dystrophy-Dystroglycanopathy (limb-Girdle), Type C, 5;
OMIM:616052 Muscular Dystrophy-Dystroglycanopathy (limb-Girdle), Type C, 7;
OMIM:618135 Muscular Dystrophy-Dystroglycanopathy (limb-Girdle), Type C, 8;
OMIM:613818 Muscular Dystrophy-Dystroglycanopathy (limb-Girdle), Type C, 9;
OMIM:309950 Muscular Dystrophy, Hemizygous Lethal Type
OMIM:603511 Muscular Dystrophy, Limb-Girdle, Autosomal Dominant 1; LGMDD1
OMIM:608423 Muscular Dystrophy, Limb-Girdle, Autosomal Dominant 2; LGMDD2
OMIM:609115 Muscular Dystrophy, Limb-Girdle, Autosomal Dominant 3; LGMDD3
OMIM:618129 Muscular Dystrophy, Limb-Girdle, Autosomal Dominant 4; LGMDD4
OMIM:608807 Muscular Dystrophy, Limb-Girdle, Autosomal Recessive 10; LGMDR10
OMIM:611307 Muscular Dystrophy, Limb-Girdle, Autosomal Recessive 12; LGMDR12
OMIM:613723 Muscular Dystrophy, Limb-Girdle, Autosomal Recessive 17; LGMDR17
OMIM:615356 Muscular Dystrophy, Limb-Girdle, Autosomal Recessive 18; LGMDR18
OMIM:253600 Muscular Dystrophy, Limb-Girdle, Autosomal Recessive 1; LGMDR1
OMIM:617232 Muscular Dystrophy, Limb-Girdle, Autosomal Recessive 21; LGMDR21
OMIM:618138 Muscular Dystrophy, Limb-Girdle, Autosomal Recessive 23; LGMDR23
OMIM:616812 Muscular Dystrophy, Limb-Girdle, Autosomal Recessive 25; LGMDR25
OMIM:618848 Muscular Dystrophy, Limb-Girdle, Autosomal Recessive 26; LGMDR26
OMIM:619566 Muscular Dystrophy, Limb-Girdle, Autosomal Recessive 27; LGMDR27
OMIM:620375 Muscular Dystrophy, Limb-Girdle, Autosomal Recessive 28; LGMDR28
OMIM:620793 Muscular Dystrophy, Limb-Girdle, Autosomal Recessive 29; LGMDR29
OMIM:253601 Muscular Dystrophy, Limb-Girdle, Autosomal Recessive 2; LGMDR2
OMIM:608099 Muscular Dystrophy, Limb-Girdle, Autosomal Recessive 3; LGMDR3
OMIM:604286 Muscular Dystrophy, Limb-Girdle, Autosomal Recessive 4; LGMDR4
OMIM:253700 Muscular Dystrophy, Limb-Girdle, Autosomal Recessive 5; LGMDR5
OMIM:601287 Muscular Dystrophy, Limb-Girdle, Autosomal Recessive 6; LGMDR6
OMIM:601954 Muscular Dystrophy, Limb-Girdle, Autosomal Recessive 7; LGMDR7
OMIM:254110 Muscular Dystrophy, Limb-Girdle, Autosomal Recessive 8; LGMDR8
OMIM:613530 Muscular Dystrophy, Limb-Girdle, Type 1H; LGMD1H
OMIM:310000 Muscular Dystrophy, Mabry Type
OMIM:310095 Muscular Dystrophy, Progressive Pectorodorsal
OMIM:159050 Muscular Dystrophy, Pseudohypertrophic, with Internalized Capillaries
OMIM:600416 Muscular Dystrophy, Scapulohumeral
OMIM:254120 Muscular Hypertonia, Lethal
OMIM:159100 Muscular Hypoplasia, Congenital Universal, of Krabbe
OMIM:254150 Musk, Inability to Smell
OMIM:610452 Mutagen Sensitivity
OMIM:249630 Mutchinick Syndrome
OMIM:254190 Myasthenia, Congenital, Refractory to Acetylcholinesterase Inhibitors
OMIM:254200 Myasthenia Gravis; MG
OMIM:607085 Myasthenia Gravis with Thymus Hyperplasia
OMIM:159400 Myasthenia, Limb-Girdle, Autoimmune
OMIM:254300 Myasthenic Syndrome, Congenital, 10; CMS10
OMIM:616326 Myasthenic Syndrome, Congenital, 11, Associated with Acetylcholine Receptor Deficiency; CMS11
OMIM:610542 Myasthenic Syndrome, Congenital, 12; CMS12
OMIM:614750 Myasthenic Syndrome, Congenital, 13; CMS13
OMIM:616228 Myasthenic Syndrome, Congenital, 14; CMS14
OMIM:616227 Myasthenic Syndrome, Congenital, 15; CMS15
OMIM:614198 Myasthenic Syndrome, Congenital, 16; CMS16
OMIM:616304 Myasthenic Syndrome, Congenital, 17; CMS17
OMIM:616330 Myasthenic Syndrome, Congenital, 18; CMS18
OMIM:616720 Myasthenic Syndrome, Congenital, 19; CMS19
OMIM:601462 Myasthenic Syndrome, Congenital, 1a, Slow-Channel; CMS1A
OMIM:608930 Myasthenic Syndrome, Congenital, 1b, Fast-Channel; CMS1B
OMIM:617143 Myasthenic Syndrome, Congenital, 20, Presynaptic; CMS20
OMIM:617239 Myasthenic Syndrome, Congenital, 21, Presynaptic; CMS21
OMIM:616224 Myasthenic Syndrome, Congenital, 22; CMS22
OMIM:618197 Myasthenic Syndrome, Congenital, 23, Presynaptic; CMS23
OMIM:618198 Myasthenic Syndrome, Congenital, 24, Presynaptic; CMS24
OMIM:618323 Myasthenic Syndrome, Congenital, 25, Presynaptic; CMS25
OMIM:616313 Myasthenic Syndrome, Congenital, 2a, Slow-Channel; CMS2A
OMIM:616314 Myasthenic Syndrome, Congenital, 2c, Associated with Acetylcholine Receptor Deficiency; CMS2C
OMIM:616321 Myasthenic Syndrome, Congenital, 3a, Slow-Channel; CMS3A
OMIM:616322 Myasthenic Syndrome, Congenital, 3b, Fast-Channel; CMS3B
OMIM:616323 Myasthenic Syndrome, Congenital, 3c, Associated with Acetylcholine Receptor Deficiency; CMS3C
OMIM:605809 Myasthenic Syndrome, Congenital, 4a, Slow-Channel; CMS4A
OMIM:616324 Myasthenic Syndrome, Congenital, 4b, Fast-Channel; CMS4B
OMIM:608931 Myasthenic Syndrome, Congenital, 4c, Associated with Acetylcholine Receptor Deficiency; CMS4C
OMIM:603034 Myasthenic Syndrome, Congenital, 5; CMS5
OMIM:254210 Myasthenic Syndrome, Congenital, 6, Presynaptic; CMS6
OMIM:616040 Myasthenic Syndrome, Congenital, 7a, Presynaptic, and Distal Motor Neuropathy, Autosomal Dominant; CMS7A
OMIM:619461 Myasthenic Syndrome, Congenital, 7b, Presynaptic, Autosomal Recessive; CMS7B
OMIM:615120 Myasthenic Syndrome, Congenital, 8; CMS8
OMIM:616325 Myasthenic Syndrome, Congenital, 9, Associated with Acetylcholine Receptor Deficiency; CMS9
OMIM:607948 Mycobacterium Tuberculosis, Susceptibility to
OMIM:607949 Mycobacterium Tuberculosis, Susceptibility to, 1
OMIM:611046 Mycobacterium Tuberculosis, Susceptibility to, 2
OMIM:612929 Mycobacterium Tuberculosis, Susceptibility to, 3
OMIM:300259 Mycobacterium Tuberculosis, Susceptibility to, X-Linked
OMIM:254400 Mycosis Fungoides
OMIM:159500 Myelinated Optic Nerve Fibers
OMIM:600080 Myelocytic Leukemia-Like Syndrome, Familial, Chronic
OMIM:601347 Myelodysplasia, Immunodeficiency, Facial Dysmorphism, Short Stature, and Psychomotor Delay
OMIM:614286 Myelodysplastic Syndrome; MDS
OMIM:254450 Myelofibrosis
OMIM:620939 Myelofibrosis, Congenital, with Anemia, Neutropenia, Developmental Delay, and Ocular Abnormalities; MFANDO
OMIM:601308 Myeloid Tumor Suppressor
OMIM:310350 Myelolymphatic Insufficiency
OMIM:254500 Myeloma, Multiple
OMIM:159580 Myelopathy, Htlv-1-Associated; HAM
OMIM:254600 Myeloperoxidase Deficiency; MPOD
OMIM:254700 Myeloproliferative Disease, Autosomal Recessive
OMIM:131440 Myeloproliferative Disorder, Chronic, with Eosinophilia
OMIM:616871 Myeloproliferative/Lymphoproliferative Neoplasms, Familial (multiple Types), Susceptibility To; MPLPF
OMIM:159595 Myeloproliferative Syndrome, Transient
OMIM:139210 Myhre Syndrome; MYHRS
OMIM:608446 Myocardial Infarction, Susceptibility to
OMIM:608557 Myocardial Infarction, Susceptibility to, 2
OMIM:616421 Myoclonic-Atonic Epilepsy; MAE
OMIM:545000 Myoclonic Epilepsy Associated with Ragged-Red Fibers; MERRF
OMIM:604363 Myoclonic Epilepsy, Congenital Deafness, Macular Dystrophy, and Psychiatric Disorders
OMIM:605021 Myoclonic Epilepsy, Familial Infantile; FIME
OMIM:159600 Myoclonic Epilepsy, Hartung Type
OMIM:608816 Myoclonic Epilepsy, Juvenile, Susceptibility to, 3; EJM3
OMIM:611364 Myoclonic Epilepsy, Juvenile, Susceptibility to, 4; EJM4
OMIM:254780 Myoclonic Epilepsy of Lafora 1; MELF1
OMIM:620681 Myoclonic Epilepsy of Lafora 2; MELF2
OMIM:254800 Myoclonic Epilepsy of Unverricht and Lundborg
OMIM:310370 Myoclonic Epilepsy, Progressive
OMIM:159800 Myoclonus, Cerebellar Ataxia, and Deafness
OMIM:614937 Myoclonus, Familial, 1; MYOCL1
OMIM:618364 Myoclonus, Familial, 2; MYOCL2
OMIM:617235 Myoclonus, Intractable, Neonatal; NEIMY
OMIM:618419 Myoectodermal Gonadal Dysgenesis Syndrome; MEGD
OMIM:619040 Myofibrillar Myopathy 10; MFM10
OMIM:619178 Myofibrillar Myopathy 11; MFM11
OMIM:228550 Myofibromatosis, Infantile, 1; IMF1
OMIM:615293 Myofibromatosis, Infantile, 2; IMF2
OMIM:268200 Myoglobinuria, Acute Recurrent, Autosomal Recessive
OMIM:160010 Myoglobinuria, Autosomal Dominant
OMIM:550500 Myoglobinuria, Recurrent
OMIM:609500 Myopathy, Autophagic Vacuolar, Infantile-Onset
OMIM:617072 Myopathy, Autosomal Recessive, with Rigid Spine and Distal Joint Contractures; MRRSDC
OMIM:160150 Myopathy, Centronuclear, 1; CNM1
OMIM:255200 Myopathy, Centronuclear, 2; CNM2
OMIM:614807 Myopathy, Centronuclear, 4; CNM4
OMIM:615959 Myopathy, Centronuclear, 5; CNM5
OMIM:617760 Myopathy, Centronuclear, 6, with Fiber-Type Disproportion; CNM6
OMIM:310400 Myopathy, Centronuclear, X-Linked; CNMX
OMIM:300580 Myopathy, Congenital, with Fiber-Type Disproportion, X-Linked; CFTDX
OMIM:160500 Myopathy, Distal, 1; MPD1
OMIM:610099 Myopathy, Distal, 3; MPD3
OMIM:614065 Myopathy, Distal, 4; MPD4
OMIM:617030 Myopathy, Distal, 5; MPD5
OMIM:618655 Myopathy, Distal, 6, Adult-Onset, Autosomal Dominant; MPD6
OMIM:301075 Myopathy, Distal, 7, Adult-Onset, X-Linked; MPD7
OMIM:160300 Myopathy, Distal, Infantile-Onset
OMIM:614321 Myopathy, Distal, Tateyama Type; MPDT
OMIM:606768 Myopathy, Distal, with Anterior Tibial Onset; DMAT
OMIM:617158 Myopathy, Distal, with Rimmed Vacuoles; DMRV
OMIM:254960 Myopathy Due to Malate-Aspartate Shuttle Defect
OMIM:615511 Myopathy Due to Myoadenylate Deaminase Deficiency; MMDD
OMIM:619036 Myopathy, Epilepsy, and Progressive Cerebral Atrophy; MEPCA
OMIM:254950 Myopathy, Granulovacuolar Lobular, with Electrical Myotonia
OMIM:616209 Myopathy, Isolated Mitochondrial, Autosomal Dominant; IMMD
OMIM:600462 Myopathy, Lactic Acidosis, and Sideroblastic Anemia 1; MLASA1
OMIM:613561 Myopathy, Lactic Acidosis, and Sideroblastic Anemia 2; MLASA2
OMIM:500011 Myopathy, Lactic Acidosis, and Sideroblastic Anemia 3; MLASA3
OMIM:617675 Myopathy, Mitochondrial, and Ataxia; MMYAT
OMIM:613076 Myopathy, Mitochondrial Progressive, with Congenital Cataract and Developmental Delay; MPMCD
OMIM:619424 Myopathy, Myofibrillar, 12, Infantile-Onset, with Cardiomyopathy;
OMIM:601419 Myopathy, Myofibrillar, 1; MFM1
OMIM:608810 Myopathy, Myofibrillar, 2; MFM2
OMIM:609200 Myopathy, Myofibrillar, 3; MFM3
OMIM:609452 Myopathy, Myofibrillar, 4; MFM4
OMIM:609524 Myopathy, Myofibrillar, 5; MFM5
OMIM:612954 Myopathy, Myofibrillar, 6; MFM6
OMIM:617114 Myopathy, Myofibrillar, 7; MFM7
OMIM:617258 Myopathy, Myofibrillar, 8; MFM8
OMIM:603689 Myopathy, Myofibrillar, 9, with Early Respiratory Failure; MFM9
OMIM:613869 Myopathy, Myofibrillar, Fatal Infantile Hypertonic, Alpha-B Crystallin-Related
OMIM:620286 Myopathy, Sarcoplasmic Body; MYOSB
OMIM:616852 Myopathy, Scapulohumeroperoneal; SHPM
OMIM:160565 Myopathy, Tubular Aggregate, 1; TAM1
OMIM:615883 Myopathy, Tubular Aggregate, 2; TAM2
OMIM:616231 Myopathy, Vacuolar, with Casq1 Aggregates; VMCQA
OMIM:615673 Myopathy with Extrapyramidal Signs; MPXPS
OMIM:255140 Myopathy with Giant Abnormal Mitochondria
OMIM:255125 Myopathy with Lactic Acidosis, Hereditary; HML
OMIM:620138 Myopathy with Myalgia, Increased Serum Creatine Kinase, and with or without Episodic Rhabdomyolysis 1; MMCKR1
OMIM:620971 Myopathy with Myalgia, Increased Serum Creatine Kinase, and with or without Episodic Rhabdomyolysis 2; MMCKR2
OMIM:601846 Myopathy with Rimmed Ubiquitin-Positive Autophagic Vacuolation, Autosomal Dominant; MRUPAV
OMIM:160570 Myopathy with Storage of Glycoproteins and Glycosaminoglycans
OMIM:310440 Myopathy, X-Linked, with Excessive Autophagy; MEAX
OMIM:300696 Myopathy, X-Linked, with Postural Muscle Atrophy; XMPMA
OMIM:609259 Myopia 10; MYP10
OMIM:609994 Myopia 11, Autosomal Dominant; MYP11
OMIM:609995 Myopia 12, Autosomal Dominant; MYP12
OMIM:300613 Myopia 13, X-Linked; MYP13
OMIM:610320 Myopia 14; MYP14
OMIM:612717 Myopia 15, Autosomal Dominant; MYP15
OMIM:612554 Myopia 16, Autosomal Dominant; MYP16
OMIM:608367 Myopia 17, Autosomal Dominant; MYP17
OMIM:255500 Myopia 18, Autosomal Recessive; MYP18
OMIM:613969 Myopia 19, Autosomal Dominant; MYP19
OMIM:310460 Myopia 1, X-Linked; MYP1
OMIM:614166 Myopia 20, Autosomal Dominant; MYP20
OMIM:614167 Myopia 21, Autosomal Dominant; MYP21
OMIM:615420 Myopia 22, Autosomal Dominant; MYP22
OMIM:615431 Myopia 23, Autosomal Recessive; MYP23
OMIM:615946 Myopia 24, Autosomal Dominant; MYP24
OMIM:617238 Myopia 25, Autosomal Dominant; MYP25
OMIM:301010 Myopia 26, X-Linked, Female-Limited; MYP26
OMIM:618827 Myopia 27, Autosomal Dominant; MYP27
OMIM:619781 Myopia 28, Autosomal Recessive; MYP28
OMIM:160700 Myopia 2, Autosomal Dominant; MYP2
OMIM:603221 Myopia 3, Autosomal Dominant; MYP3
OMIM:608474 Myopia 5, Autosomal Dominant; MYP5
OMIM:608908 Myopia 6; MYP6
OMIM:609256 Myopia 7; MYP7
OMIM:609257 Myopia 8; MYP8
OMIM:609258 Myopia 9; MYP9
OMIM:614292 Myopia, High, with Cataract and Vitreoretinal Degeneration; MCVD
OMIM:255600 Myosclerosis, Autosomal Recessive
OMIM:160750 Myositis
OMIM:160800 Myotonia Congenita, Autosomal Dominant
OMIM:255700 Myotonia Congenita, Autosomal Recessive
OMIM:608390 Myotonia, Potassium-Aggravated
OMIM:255710 Myotonia with Skeletal Abnormalities and Impaired Intellectual Development
OMIM:160900 Myotonic Dystrophy 1; DM1
OMIM:602668 Myotonic Dystrophy 2; DM2
OMIM:160990 Myotonic Myopathy with Cylindrical Spirals
OMIM:300219 Myotubular Myopathy with Abnormal Genital Development
OMIM:255900 Myxedema
OMIM:613488 Myxoid Liposarcoma
OMIM:255960 Myxoma, Intracardiac
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