About   Help   FAQ
Human Disease Vocabulary Browser
The current vocabulary contains human disease, syndrome, and condition terms from Online Mendelian Inheritance in Man (OMIM database).
Browse vocabulary terms by beginning character
 
A B C D E F G H I J K L M N O P Q R S T U V W X Y Z 0-9
 
Human Diseases/Syndromes Beginning with "I"

To see all annotations for a disease, click the disease name.

OMIM IDHuman Disease
OMIM:308200 Ichthyosis and Male Hypogonadism
OMIM:607602 Ichthyosis, Annular Epidermolytic, 1; AEI1
OMIM:620148 Ichthyosis, Annular Epidermolytic, 2; AEI2
OMIM:146800 Ichthyosis Bullosa of Siemens; IBS
OMIM:146720 Ichthyosis--Cheek--Eyebrow Syndrome
OMIM:615024 Ichthyosis, Congenital, Autosomal Recessive 10; ARCI10
OMIM:602400 Ichthyosis, Congenital, Autosomal Recessive 11; ARCI11
OMIM:617320 Ichthyosis, Congenital, Autosomal Recessive 12; ARCI12
OMIM:617574 Ichthyosis, Congenital, Autosomal Recessive 13; ARCI13
OMIM:617571 Ichthyosis, Congenital, Autosomal Recessive 14; ARCI14
OMIM:242300 Ichthyosis, Congenital, Autosomal Recessive 1; ARCI1
OMIM:242100 Ichthyosis, Congenital, Autosomal Recessive 2; ARCI2
OMIM:606545 Ichthyosis, Congenital, Autosomal Recessive 3; ARCI3
OMIM:601277 Ichthyosis, Congenital, Autosomal Recessive 4A; ARCI4A
OMIM:242500 Ichthyosis, Congenital, Autosomal Recessive 4b; ARCI4B
OMIM:604777 Ichthyosis, Congenital, Autosomal Recessive 5; ARCI5
OMIM:612281 Ichthyosis, Congenital, Autosomal Recessive 6; ARCI6
OMIM:615022 Ichthyosis, Congenital, Autosomal Recessive 7; ARCI7
OMIM:613943 Ichthyosis, Congenital, Autosomal Recessive 8; ARCI8
OMIM:615023 Ichthyosis, Congenital, Autosomal Recessive 9; ARCI9
OMIM:242400 Ichthyosis Congenita with Biliary Atresia
OMIM:242520 Ichthyosis, Hepatosplenomegaly, and Cerebellar Degeneration
OMIM:146590 Ichthyosis Hystrix, Curth-Macklin Type; IHCM
OMIM:146600 Ichthyosis Hystrix, Lambert Type; IHL
OMIM:602540 Ichthyosis, Hystrix-Like, with Deafness
OMIM:601039 Ichthyosis-Impaired Intellectual Developmental Syndrome with Large Keratohyalin Granules in the Skin
OMIM:242530 Ichthyosis, Impaired Intellectual Development, Dwarfism, and Renal Impairment
OMIM:146750 Ichthyosis, Lamellar, Autosomal Dominant; ADLI
OMIM:607626 Ichthyosis, Leukocyte Vacuoles, Alopecia, and Sclerosing Cholangitis;
OMIM:608649 Ichthyosis Prematurity Syndrome; IPS
OMIM:614457 Ichthyosis, Spastic Quadriplegia, and Impaired Intellectual Development; ISQMR
OMIM:242550 Ichthyosis, Split Hairs, and Amino Aciduria
OMIM:146700 Ichthyosis Vulgaris
OMIM:242510 Ichthyosis with Alopecia, Eclabium, Ectropion, and Impaired Intellectual Development
OMIM:609165 Ichthyosis with Confetti; IWC
OMIM:620507 Ichthyosis with Erythrokeratoderma; IEKD
OMIM:300001 Ichthyosis, X-Linked, without Steroid Sulfatase Deficiency
OMIM:308100 Ichthyosis, X-Linked; XLI
OMIM:618527 Ichthyotic Keratoderma, Spasticity, Hypomyelination, and Dysmorphic Facial Features; IKSHD
OMIM:308205 Ifap Syndrome 1, with or without Bresheck Syndrome; IFAP1
OMIM:619016 Ifap Syndrome 2; IFAP2
OMIM:161950 Iga Nephropathy, Susceptibility to, 1; IGAN1
OMIM:613944 Iga Nephropathy, Susceptibility to, 2; IGAN2
OMIM:616818 Iga Nephropathy, Susceptibility to, 3; IGAN3
OMIM:147050 IgE Responsiveness, Atopic; IGER
OMIM:208155 Illum Syndrome
OMIM:618786 Imagawa-Matsumoto Syndrome; IMMAS
OMIM:261100 Imerslund-Grasbeck Syndrome 1; IGS1
OMIM:618882 Imerslund-Grasbeck Syndrome 2; IGS2
OMIM:242600 Iminoglycinuria
OMIM:242850 Immune Deficiency Disease
OMIM:146830 Immune Deficiency, Familial Variable
OMIM:618998 Immune Dysregulation and Systemic Hyperinflammation Syndrome; IMDYSHI
OMIM:620514 Immune Dysregulation, Autoimmunity, and Autoinflammation; IDAA
OMIM:616100 Immune Dysregulation with Autoimmunity, Immunodeficiency, and Lymphoproliferation; IDAIL
OMIM:146850 Immune Suppression; IS
OMIM:188030 Immune Thrombocytopenia; ITP
OMIM:618042 Immunodeficiency 100 with Pulmonary Alveolar Proteinosis and Hypogammaglobulinemia; IMD100
OMIM:619872 Immunodeficiency 101 (varicella Zoster Virus-Specific); IMD101
OMIM:301082 Immunodeficiency 102; IMD102
OMIM:212050 Immunodeficiency 103, Susceptibility to Fungal Infections; IMD103
OMIM:608971 Immunodeficiency 104, Severe Combined; IMD104
OMIM:619924 Immunodeficiency 105, Severe Combined; IMD105
OMIM:619935 Immunodeficiency 106, Susceptibility to Viral Infections; IMD106
OMIM:619986 Immunodeficiency 107, Susceptibility to Invasive Staphylococcus Aureus Infection; IMD107
OMIM:260570 Immunodeficiency 108 with Autoinflammation; IMD108
OMIM:620282 Immunodeficiency 109 with Lymphoproliferation; IMD109
OMIM:612783 Immunodeficiency 10; IMD10
OMIM:614868 Immunodeficiency 110 with Lymphoproliferation; IMD110
OMIM:620449 Immunodeficiency 112; IMD112
OMIM:620565 Immunodeficiency 113 with Autoimmunity and Autoinflammation; IMD113
OMIM:620603 Immunodeficiency 114, Folate-Responsive; IMD114
OMIM:620632 Immunodeficiency 115 with Autoinflammation; IMD115
OMIM:608957 Immunodeficiency 116; IMD116
OMIM:620668 Immunodeficiency 117; IMD117
OMIM:301115 Immunodeficiency 118; IMD118
OMIM:620825 Immunodeficiency 119; IMD119
OMIM:615206 Immunodeficiency 11a; IMD11A
OMIM:617638 Immunodeficiency 11b with Atopic Dermatitis; IMD11B
OMIM:620836 Immunodeficiency 120; IMD120
OMIM:620807 Immunodeficiency 121 with Autoinflammation; IMD121
OMIM:620869 Immunodeficiency 122; IMD122
OMIM:620901 Immunodeficiency 123 with Hpv-Related Verrucosis; IMD123
OMIM:611291 Immunodeficiency 124, Severe Combined; IMD124
OMIM:620926 Immunodeficiency 125; IMD125
OMIM:620931 Immunodeficiency 126, Susceptibility To; IMD126
OMIM:620977 Immunodeficiency 127; IMD127
OMIM:620983 Immunodeficiency 128; IMD128
OMIM:615468 Immunodeficiency 12; IMD12
OMIM:615518 Immunodeficiency 13; IMD13
OMIM:615513 Immunodeficiency 14a with Lymphoproliferation, Autosomal Dominant;
OMIM:619281 Immunodeficiency 14b, Autosomal Recessive; IMD14B
OMIM:618204 Immunodeficiency 15a; IMD15A
OMIM:615592 Immunodeficiency 15b; IMD15B
OMIM:615593 Immunodeficiency 16; IMD16
OMIM:615607 Immunodeficiency 17; IMD17
OMIM:615615 Immunodeficiency 18; IMD18
OMIM:615617 Immunodeficiency 19, Severe Combined; IMD19
OMIM:615707 Immunodeficiency 20; IMD20
OMIM:614172 Immunodeficiency 21; IMD21
OMIM:615758 Immunodeficiency 22; IMD22
OMIM:615816 Immunodeficiency 23; IMD23
OMIM:615897 Immunodeficiency 24; IMD24
OMIM:610163 Immunodeficiency 25; IMD25
OMIM:615966 Immunodeficiency 26 with or without Neurologic Abnormalities; IMD26
OMIM:209950 Immunodeficiency 27a; IMD27A
OMIM:615978 Immunodeficiency 27b; IMD27B
OMIM:614889 Immunodeficiency 28; IMD28
OMIM:614890 Immunodeficiency 29; IMD29
OMIM:614891 Immunodeficiency 30; IMD30
OMIM:614892 Immunodeficiency 31a; IMD31A
OMIM:613796 Immunodeficiency 31b; IMD31B
OMIM:614162 Immunodeficiency 31c; IMD31C
OMIM:614893 Immunodeficiency 32a; IMD32A
OMIM:226990 Immunodeficiency 32b; IMD32B
OMIM:300636 Immunodeficiency 33; IMD33
OMIM:300645 Immunodeficiency 34; IMD34
OMIM:611521 Immunodeficiency 35; IMD35
OMIM:616005 Immunodeficiency 36 with Lymphoproliferation; IMD36
OMIM:616098 Immunodeficiency 37; IMD37
OMIM:616126 Immunodeficiency 38 with Basal Ganglia Calcification; IMD38
OMIM:616345 Immunodeficiency 39; IMD39
OMIM:616433 Immunodeficiency 40; IMD40
OMIM:606367 Immunodeficiency 41 with Lymphoproliferation and Autoimmunity; IMD41
OMIM:616622 Immunodeficiency 42; IMD42
OMIM:241600 Immunodeficiency 43; IMD43
OMIM:616636 Immunodeficiency 44; IMD44
OMIM:616669 Immunodeficiency 45; IMD45
OMIM:616740 Immunodeficiency 46; IMD46
OMIM:300972 Immunodeficiency 47; IMD47
OMIM:269840 Immunodeficiency 48; IMD48
OMIM:617237 Immunodeficiency 49, Severe Combined; IMD49
OMIM:300988 Immunodeficiency 50; IMD50
OMIM:613953 Immunodeficiency 51; IMD51
OMIM:617514 Immunodeficiency 52; IMD52
OMIM:617585 Immunodeficiency 53; IMD53
OMIM:609981 Immunodeficiency 54; IMD54
OMIM:617827 Immunodeficiency 55; IMD55
OMIM:615207 Immunodeficiency 56; IMD56
OMIM:618108 Immunodeficiency 57 with Autoinflammation; IMD57
OMIM:618131 Immunodeficiency 58; IMD58
OMIM:233600 Immunodeficiency 59 and Hypoglycemia; IMD59
OMIM:618394 Immunodeficiency 60 and Autoimmunity; IMD60
OMIM:300310 Immunodeficiency 61; IMD61
OMIM:618459 Immunodeficiency 62; IMD62
OMIM:618495 Immunodeficiency 63 with Lymphoproliferation and Autoimmunity; IMD63
OMIM:618534 Immunodeficiency 64 with Lymphoproliferation; IMD64
OMIM:618648 Immunodeficiency 65, Susceptibility to Viral Infections; IMD65
OMIM:618847 Immunodeficiency 66; IMD66
OMIM:607676 Immunodeficiency 67; IMD67
OMIM:612260 Immunodeficiency 68; IMD68
OMIM:618963 Immunodeficiency 69; IMD69
OMIM:618969 Immunodeficiency 70; IMD70
OMIM:617718 Immunodeficiency 71 with Inflammatory Disease and Congenital Thrombocytopenia; IMD71
OMIM:618982 Immunodeficiency 72 with Autoinflammation and Lymphoproliferation;
OMIM:608203 Immunodeficiency 73a with Defective Neutrophil Chemotaxis and Leukocytosis; IMD73A
OMIM:618986 Immunodeficiency 73b with Defective Neutrophil Chemotaxis and Lymphopenia; IMD73B
OMIM:618987 Immunodeficiency 73c with Defective Neutrophil Chemotaxis and Hypogammaglobulinemia; IMD73C
OMIM:301051 Immunodeficiency 74, Covid19-Related, X-Linked; IMD74
OMIM:619126 Immunodeficiency 75 with Lymphoproliferation; IMD75
OMIM:619164 Immunodeficiency 76; IMD76
OMIM:619223 Immunodeficiency 77; IMD77
OMIM:619220 Immunodeficiency 78 with Autoimmunity and Developmental Delay; IMD78
OMIM:619238 Immunodeficiency 79; IMD79
OMIM:615387 Immunodeficiency 7; IMD7
OMIM:619313 Immunodeficiency 80 with or without Congenital Cardiomyopathy; IMD80
OMIM:619374 Immunodeficiency 81; IMD81
OMIM:619381 Immunodeficiency 82 with Systemic Inflammation; IMD82
OMIM:613002 Immunodeficiency 83, Susceptibility to Viral Infections; IMD83
OMIM:619437 Immunodeficiency 84; IMD84
OMIM:619510 Immunodeficiency 85 and Autoimmunity; IMD85
OMIM:619549 Immunodeficiency 86; IMD86
OMIM:619573 Immunodeficiency 87 and Autoimmunity; IMD87
OMIM:619630 Immunodeficiency 88; IMD88
OMIM:619632 Immunodeficiency 89 and Autoimmunity; IMD89
OMIM:615401 Immunodeficiency 8 with Lymphoproliferation; IMD8
OMIM:613759 Immunodeficiency 90 with Encephalopathy, Functional Hyposplenia, and Hepatic Dysfunction; IMD90
OMIM:619644 Immunodeficiency 91 and Hyperinflammation; IMD91
OMIM:619652 Immunodeficiency 92; IMD92
OMIM:619705 Immunodeficiency 93 and Hypertrophic Cardiomyopathy; IMD93
OMIM:619750 Immunodeficiency 94 with Autoinflammation and Dysmorphic Facies;
OMIM:619773 Immunodeficiency 95; IMD95
OMIM:619774 Immunodeficiency 96; IMD96
OMIM:619802 Immunodeficiency 97 with Autoinflammation; IMD97
OMIM:301078 Immunodeficiency 98 with Autoinflammation, X-Linked; IMD98
OMIM:619846 Immunodeficiency 99 with Hypogammaglobulinemia and Autoimmune Cytopenias; IMD99
OMIM:612782 Immunodeficiency 9; IMD9
OMIM:242860 Immunodeficiency-Centromeric Instability-Facial Anomalies Syndrome 1;
OMIM:614069 Immunodeficiency-Centromeric Instability-Facial Anomalies Syndrome 2;
OMIM:616910 Immunodeficiency-Centromeric Instability-Facial Anomalies Syndrome 3;
OMIM:616911 Immunodeficiency-Centromeric Instability-Facial Anomalies Syndrome 4;
OMIM:615577 Immunodeficiency, Common Variable, 10; CVID10
OMIM:615767 Immunodeficiency, Common Variable, 11; CVID11
OMIM:616576 Immunodeficiency, Common Variable, 12, with Autoimmunity; CVID12
OMIM:616873 Immunodeficiency, Common Variable, 13; CVID13
OMIM:617765 Immunodeficiency, Common Variable, 14; CVID14
OMIM:620670 Immunodeficiency, Common Variable, 15; CVID15
OMIM:607594 Immunodeficiency, Common Variable, 1; CVID1
OMIM:240500 Immunodeficiency, Common Variable, 2; CVID2
OMIM:613493 Immunodeficiency, Common Variable, 3; CVID3
OMIM:613494 Immunodeficiency, Common Variable, 4; CVID4
OMIM:613495 Immunodeficiency, Common Variable, 5; CVID5
OMIM:613496 Immunodeficiency, Common Variable, 6; CVID6
OMIM:614699 Immunodeficiency, Common Variable, 7; CVID7
OMIM:614700 Immunodeficiency, Common Variable, 8, with Autoimmunity; CVID8
OMIM:617744 Immunodeficiency, Developmental Delay, and Hypohomocysteinemia;
OMIM:610798 Immunodeficiency Due to Defect in Mapbp-Interacting Protein
OMIM:611926 Immunodeficiency, Ovarian Dysgenesis, and Pulmonary Fibrosis
OMIM:243110 Immunodeficiency with Defective T-Cell Response to Interleukin 1
OMIM:308230 Immunodeficiency with Hyper-IgM, Type 1; HIGM1
OMIM:605258 Immunodeficiency with Hyper-Igm, Type 2; HIGM2
OMIM:606843 Immunodeficiency with Hyper-Igm, Type 3; HIGM3
OMIM:608184 Immunodeficiency with Hyper-Igm, Type 4; HIGM4
OMIM:608106 Immunodeficiency with Hyper-Igm, Type 5; HIGM5
OMIM:308220 Immunodeficiency, X-Linked, with Deficiency of 115,000 Dalton Surface Glycoprotein
OMIM:300853 Immunodeficiency, X-Linked, with Magnesium Defect, Epstein-Barr Virus Infection, and Neoplasia; XMEN
OMIM:304790 Immunodysregulation, Polyendocrinopathy, and Enteropathy, X-Linked;
OMIM:242880 Immunoerythromyeloid Hypoplasia
OMIM:137100 Immunoglobulin A Deficiency 1; IGAD1
OMIM:609529 Immunoglobulin A Deficiency 2; IGAD2
OMIM:242890 Immunoglobulin D Level in Plasma, Low
OMIM:614102 Immunoglobulin Kappa Light Chain Deficiency; IGKCD
OMIM:308250 Immunoglobulin M, Level of
OMIM:147260 Immunoglobulin Switch Sequences
OMIM:300076 Immunoneurologic Disorder, X-Linked
OMIM:617425 Immunoskeletal Dysplasia with Neurodevelopmental Abnormalities; ISDNA
OMIM:308280 Impacted Teeth, Multiple
OMIM:616789 Impaired Intellectual Development and Distinctive Facial Features with or without Cardiac Defects; MRFACD
OMIM:309480 Impaired Intellectual Development and Psoriasis
OMIM:613671 Impaired Intellectual Development, Anterior Maxillary Protrusion, and Strabismus; MRAMS
OMIM:601352 Impaired Intellectual Development, Microcephaly, Epilepsy, and Coarse Face
OMIM:606772 Impaired Intellectual Development, Obesity, Mandibular Prognathism, and Eye and Skin Anomalies
OMIM:610156 Impaired Intellectual Development, Truncal Obesity, Retinal Dystrophy, and Micropenis Syndrome; MORMS
OMIM:309560 Impaired Intellectual Development with Spastic Paraplegia and Palmoplantar Hyperkeratosis
OMIM:617995 Impdh2 Enzyme Activity, Variation In; IMPDH2V
OMIM:308290 Imprinting Gene Related to Retinoblastoma
OMIM:147251 Incisors, Fused Mandibular
OMIM:147300 Incisors, Long Upper Central
OMIM:147330 Incisors, Lower Central, Absence of
OMIM:147350 Incisors, Rotation of Upper Central
OMIM:147400 Incisors, Shovel-Shaped
OMIM:619733 Inclusion Body Myopathy and Brain White Matter Abnormalities; IBMWMA
OMIM:167320 Inclusion Body Myopathy with Early-Onset Paget Disease with or without Frontotemporal Dementia 1; IBMPFD1
OMIM:615422 Inclusion Body Myopathy with Early-Onset Paget Disease with or without Frontotemporal Dementia 2; IBMPFD2
OMIM:615424 Inclusion Body Myopathy with Early-Onset Paget Disease with or without Frontotemporal Dementia 3; IBMPFD3
OMIM:147421 Inclusion Body Myositis
OMIM:308300 Incontinentia Pigmenti; IP
OMIM:243000 Indifference to Pain, Congenital, Autosomal Recessive; CIP
OMIM:243050 Indolylacroyl Glycinuria with Impaired Intellectual Development
OMIM:618339 Infantile Cataract, Skin Abnormalities, Glutamate Excess, and Impaired Intellectual Development; CASGID
OMIM:614559 Infantile Cerebellar-Retinal Degeneration; ICRD
OMIM:615438 Infantile Liver Failure Syndrome 1; ILFS1
OMIM:616483 Infantile Liver Failure Syndrome 2; ILFS2
OMIM:618641 Infantile Liver Failure Syndrome 3; ILFS3
OMIM:269920 Infantile Sialic Acid Storage Disease; ISSD
OMIM:191390 Inflammatory Bowel Disease 11; IBD11
OMIM:612241 Inflammatory Bowel Disease 12; IBD12
OMIM:612244 Inflammatory Bowel Disease 13; IBD13
OMIM:612245 Inflammatory Bowel Disease 14; IBD14
OMIM:612255 Inflammatory Bowel Disease 15; IBD15
OMIM:612259 Inflammatory Bowel Disease 16; IBD16
OMIM:612261 Inflammatory Bowel Disease 17; IBD17
OMIM:612262 Inflammatory Bowel Disease 18; IBD18
OMIM:612288 Inflammatory Bowel Disease 20; IBD20
OMIM:612354 Inflammatory Bowel Disease 21; IBD21
OMIM:612380 Inflammatory Bowel Disease 22; IBD22
OMIM:612381 Inflammatory Bowel Disease 23; IBD23
OMIM:612566 Inflammatory Bowel Disease 24; IBD24
OMIM:612567 Inflammatory Bowel Disease 25, Autosomal Recessive; IBD25
OMIM:612639 Inflammatory Bowel Disease 26; IBD26
OMIM:612796 Inflammatory Bowel Disease 27; IBD27
OMIM:613148 Inflammatory Bowel Disease 28, Autosomal Recessive; IBD28
OMIM:618077 Inflammatory Bowel Disease 29; IBD29
OMIM:601458 Inflammatory Bowel Disease 2; IBD2
OMIM:604519 Inflammatory Bowel Disease 3; IBD3
OMIM:606675 Inflammatory Bowel Disease 4; IBD4
OMIM:606348 Inflammatory Bowel Disease 5; IBD5
OMIM:606674 Inflammatory Bowel Disease 6; IBD6
OMIM:605225 Inflammatory Bowel Disease 7; IBD7
OMIM:606668 Inflammatory Bowel Disease 8; IBD8
OMIM:608448 Inflammatory Bowel Disease 9; IBD9
OMIM:611081 Inflammatory Bowel Disease (crohn Disease) 10; IBD10
OMIM:612278 Inflammatory Bowel Disease (crohn Disease) 19; IBD19
OMIM:266600 Inflammatory Bowel Disease (crohn Disease) 1; IBD1
OMIM:619079 Inflammatory Bowel Disease (crohn Disease) 30; IBD30
OMIM:618213 Inflammatory Bowel Disease, Immunodeficiency, and Encephalopathy;
OMIM:619398 Inflammatory Bowel Disease (infantile Ulcerative Colitis) 31, Autosomal Recessive; IBD31
OMIM:620199 Inflammatory Poikiloderma with Hair Abnormalities and Acral Keratoses; IPHAK
OMIM:614328 Inflammatory Skin and Bowel Disease, Neonatal, 1; NISBD1
OMIM:614680 Influenza, Severe, Susceptibility to
OMIM:600989 Infundibulopelvic Dysgenesis
OMIM:243080 Inosine Phosphorylase Deficiency, Immune Defect Due to
OMIM:613850 Inosine Triphosphatase Deficiency
OMIM:147540 Insect Stings, Hypersensitivity to
OMIM:256800 Insensitivity to Pain, Congenital, with Anhidrosis; CIPA
OMIM:147530 Insensitivity to Pain with Hyperplastic Myelinopathy
OMIM:608747 Insulin-Like Growth Factor I Deficiency; IGF1D
OMIM:270450 Insulin-Like Growth Factor I, Resistance To; IGF1RES
OMIM:147630 Insulinomatosis and Diabetes Mellitus; INSDM
OMIM:606960 Insulinoma Tumor Suppressor Gene Locus
OMIM:147320 Insulin Receptors, Familial Increase in
OMIM:618195 Intellectual Developmental Disorder and Retinitis Pigmentosa; IDDRP
OMIM:614256 Intellectual Developmental Disorder, Autosomal Dominant 10; MRD10
OMIM:156200 Intellectual Developmental Disorder, Autosomal Dominant 1; MRD1
OMIM:615502 Intellectual Developmental Disorder, Autosomal Dominant 21; MRD21
OMIM:612337 Intellectual Developmental Disorder, Autosomal Dominant 22; MRD22
OMIM:615761 Intellectual Developmental Disorder, Autosomal Dominant 23; MRD23
OMIM:615834 Intellectual Developmental Disorder, Autosomal Dominant 26; MRD26
OMIM:616078 Intellectual Developmental Disorder, Autosomal Dominant 29; MRD29
OMIM:614113 Intellectual Developmental Disorder, Autosomal Dominant 2; MRD2
OMIM:616083 Intellectual Developmental Disorder, Autosomal Dominant 30, with Speech Delay and Behavioral Abnormalities; MRD30
OMIM:616311 Intellectual Developmental Disorder, Autosomal Dominant 33; MRD33
OMIM:616351 Intellectual Developmental Disorder, Autosomal Dominant 34; MRD34
OMIM:616393 Intellectual Developmental Disorder, Autosomal Dominant 38; MRD38
OMIM:616521 Intellectual Developmental Disorder, Autosomal Dominant 39; MRD39
OMIM:612580 Intellectual Developmental Disorder, Autosomal Dominant 3; MRD3
OMIM:616944 Intellectual Developmental Disorder, Autosomal Dominant 41; MRD41
OMIM:616973 Intellectual Developmental Disorder, Autosomal Dominant 42; MRD42
OMIM:616977 Intellectual Developmental Disorder, Autosomal Dominant 43; MRD43
OMIM:617061 Intellectual Developmental Disorder, Autosomal Dominant 44, with Microcephaly; MRD44
OMIM:617600 Intellectual Developmental Disorder, Autosomal Dominant 45; MRD45
OMIM:617601 Intellectual Developmental Disorder, Autosomal Dominant 46; MRD46
OMIM:617635 Intellectual Developmental Disorder, Autosomal Dominant 47; MRD47
OMIM:617751 Intellectual Developmental Disorder, Autosomal Dominant 48; MRD48
OMIM:612581 Intellectual Developmental Disorder, Autosomal Dominant 4; MRD4
OMIM:617787 Intellectual Developmental Disorder, Autosomal Dominant 50, with Behavioral Abnormalities; MRD50
OMIM:617788 Intellectual Developmental Disorder, Autosomal Dominant 51; MRD51
OMIM:617796 Intellectual Developmental Disorder, Autosomal Dominant 52; MRD52
OMIM:617798 Intellectual Developmental Disorder, Autosomal Dominant 53; MRD53
OMIM:617799 Intellectual Developmental Disorder, Autosomal Dominant 54; MRD54
OMIM:617831 Intellectual Developmental Disorder, Autosomal Dominant 55, with Seizures; MRD55
OMIM:617854 Intellectual Developmental Disorder, Autosomal Dominant 56; MRD56
OMIM:618050 Intellectual Developmental Disorder, Autosomal Dominant 57; MRD57
OMIM:618106 Intellectual Developmental Disorder, Autosomal Dominant 58; MRD58
OMIM:618522 Intellectual Developmental Disorder, Autosomal Dominant 59; MRD59
OMIM:612621 Intellectual Developmental Disorder, Autosomal Dominant 5; MRD5
OMIM:618587 Intellectual Developmental Disorder, Autosomal Dominant 60, with Seizures; MRD60
OMIM:618009 Intellectual Developmental Disorder, Autosomal Dominant 61; MRD61
OMIM:618793 Intellectual Developmental Disorder, Autosomal Dominant 62; MRD62
OMIM:618825 Intellectual Developmental Disorder, Autosomal Dominant 63, with Macrocephaly; MRD63
OMIM:619188 Intellectual Developmental Disorder, Autosomal Dominant 64; MRD64
OMIM:619320 Intellectual Developmental Disorder, Autosomal Dominant 65; MRD65
OMIM:619910 Intellectual Developmental Disorder, Autosomal Dominant 66; MRD66
OMIM:619927 Intellectual Developmental Disorder, Autosomal Dominant 67; MRD67
OMIM:619934 Intellectual Developmental Disorder, Autosomal Dominant 68; MRD68
OMIM:617863 Intellectual Developmental Disorder, Autosomal Dominant 69; MRD69
OMIM:613970 Intellectual Developmental Disorder, Autosomal Dominant 6, with or without Seizures; MRD6
OMIM:620157 Intellectual Developmental Disorder, Autosomal Dominant 70; MRD70
OMIM:620330 Intellectual Developmental Disorder, Autosomal Dominant 71, with Behavioral Abnormalities; MRD71
OMIM:620439 Intellectual Developmental Disorder, Autosomal Dominant 72; MRD72
OMIM:620450 Intellectual Developmental Disorder, Autosomal Dominant 73; MRD73
OMIM:620688 Intellectual Developmental Disorder, Autosomal Dominant 74; MRD74
OMIM:620988 Intellectual Developmental Disorder, Autosomal Dominant 75; MRD75
OMIM:614104 Intellectual Developmental Disorder, Autosomal Dominant 7; MRD7
OMIM:611096 Intellectual Developmental Disorder, Autosomal Recessive 10; MRT10
OMIM:611097 Intellectual Developmental Disorder, Autosomal Recessive 11; MRT11
OMIM:611090 Intellectual Developmental Disorder, Autosomal Recessive 12; MRT12
OMIM:613192 Intellectual Developmental Disorder, Autosomal Recessive 13; MRT13
OMIM:614020 Intellectual Developmental Disorder, Autosomal Recessive 14; MRT14
OMIM:614208 Intellectual Developmental Disorder, Autosomal Recessive 16; MRT16
OMIM:614249 Intellectual Developmental Disorder, Autosomal Recessive 18, with or without Epilepsy; MRT18
OMIM:614343 Intellectual Developmental Disorder, Autosomal Recessive 19; MRT19
OMIM:249500 Intellectual Developmental Disorder, Autosomal Recessive 1; MRT1
OMIM:614344 Intellectual Developmental Disorder, Autosomal Recessive 23; MRT23
OMIM:614345 Intellectual Developmental Disorder, Autosomal Recessive 24; MRT24
OMIM:614346 Intellectual Developmental Disorder, Autosomal Recessive 25; MRT25
OMIM:614340 Intellectual Developmental Disorder, Autosomal Recessive 27; MRT27
OMIM:614347 Intellectual Developmental Disorder, Autosomal Recessive 28; MRT28
OMIM:614333 Intellectual Developmental Disorder, Autosomal Recessive 29; MRT29
OMIM:607417 Intellectual Developmental Disorder, Autosomal Recessive 2; MRT2
OMIM:614342 Intellectual Developmental Disorder, Autosomal Recessive 30; MRT30
OMIM:614329 Intellectual Developmental Disorder, Autosomal Recessive 31; MRT31
OMIM:614341 Intellectual Developmental Disorder, Autosomal Recessive 33; MRT33
OMIM:614499 Intellectual Developmental Disorder, Autosomal Recessive 34, with Variant Lissencephaly; MRT34
OMIM:615162 Intellectual Developmental Disorder, Autosomal Recessive 35; MRT35
OMIM:615493 Intellectual Developmental Disorder, Autosomal Recessive 37; MRT37
OMIM:615516 Intellectual Developmental Disorder, Autosomal Recessive 38; MRT38
OMIM:615541 Intellectual Developmental Disorder, Autosomal Recessive 39; MRT39
OMIM:608443 Intellectual Developmental Disorder, Autosomal Recessive 3; MRT3
OMIM:615637 Intellectual Developmental Disorder, Autosomal Recessive 41; MRT41
OMIM:615817 Intellectual Developmental Disorder, Autosomal Recessive 43; MRT43
OMIM:615942 Intellectual Developmental Disorder, Autosomal Recessive 44; MRT44
OMIM:615979 Intellectual Developmental Disorder, Autosomal Recessive 45; MRT45
OMIM:616116 Intellectual Developmental Disorder, Autosomal Recessive 46; MRT46
OMIM:616193 Intellectual Developmental Disorder, Autosomal Recessive 47; MRT47
OMIM:616269 Intellectual Developmental Disorder, Autosomal Recessive 48; MRT48
OMIM:611107 Intellectual Developmental Disorder, Autosomal Recessive 4; MRT4
OMIM:616460 Intellectual Developmental Disorder, Autosomal Recessive 50; MRT50
OMIM:616739 Intellectual Developmental Disorder, Autosomal Recessive 51; MRT51
OMIM:616887 Intellectual Developmental Disorder, Autosomal Recessive 52; MRT52
OMIM:617028 Intellectual Developmental Disorder, Autosomal Recessive 54; MRT54
OMIM:617125 Intellectual Developmental Disorder, Autosomal Recessive 56; MRT56
OMIM:617188 Intellectual Developmental Disorder, Autosomal Recessive 57; MRT57
OMIM:617270 Intellectual Developmental Disorder, Autosomal Recessive 58; MRT58
OMIM:617323 Intellectual Developmental Disorder, Autosomal Recessive 59; MRT59
OMIM:611091 Intellectual Developmental Disorder, Autosomal Recessive 5; MRT5
OMIM:617432 Intellectual Developmental Disorder, Autosomal Recessive 60; MRT60
OMIM:617773 Intellectual Developmental Disorder, Autosomal Recessive 61; MRT61
OMIM:618095 Intellectual Developmental Disorder, Autosomal Recessive 63; MRT63
OMIM:618103 Intellectual Developmental Disorder, Autosomal Recessive 64; MRT64
OMIM:618109 Intellectual Developmental Disorder, Autosomal Recessive 65; MRT65
OMIM:618221 Intellectual Developmental Disorder, Autosomal Recessive 66; MRT66
OMIM:618295 Intellectual Developmental Disorder, Autosomal Recessive 67; MRT67
OMIM:618302 Intellectual Developmental Disorder, Autosomal Recessive 68; MRT68
OMIM:611092 Intellectual Developmental Disorder, Autosomal Recessive 6; MRT6
OMIM:618402 Intellectual Developmental Disorder, Autosomal Recessive 70; MRT70
OMIM:618504 Intellectual Developmental Disorder, Autosomal Recessive 71; MRT71
OMIM:618665 Intellectual Developmental Disorder, Autosomal Recessive 72; MRT72
OMIM:619717 Intellectual Developmental Disorder, Autosomal Recessive 73; MRT73
OMIM:617169 Intellectual Developmental Disorder, Autosomal Recessive 74; MRT74
OMIM:619827 Intellectual Developmental Disorder, Autosomal Recessive 75, with Neuropsychiatric Features and Variant Lissencephaly; MRT75
OMIM:619931 Intellectual Developmental Disorder, Autosomal Recessive 76; MRT76
OMIM:619988 Intellectual Developmental Disorder, Autosomal Recessive 77; MRT77
OMIM:620237 Intellectual Developmental Disorder, Autosomal Recessive 78; MRT78
OMIM:620393 Intellectual Developmental Disorder, Autosomal Recessive 79; MRT79
OMIM:611093 Intellectual Developmental Disorder, Autosomal Recessive 7; MRT7
OMIM:620653 Intellectual Developmental Disorder, Autosomal Recessive 80, with Variant Lissencephaly; MRT80
OMIM:620700 Intellectual Developmental Disorder, Autosomal Recessive 81; MRT81
OMIM:620779 Intellectual Developmental Disorder, Autosomal Recessive 82; MRT82
OMIM:611095 Intellectual Developmental Disorder, Autosomal Recessive 9; MRT9
OMIM:249599 Intellectual Developmental Disorder, Belgian Type
OMIM:136630 Intellectual Developmental Disorder, Fra12a Type
OMIM:618342 Intellectual Developmental Disorder with Abnormal Behavior, Microcephaly, and Short Stature; IDDABS
OMIM:620021 Intellectual Developmental Disorder with Autism and Dysmorphic Facies; IDDADF
OMIM:615032 Intellectual Developmental Disorder with Autism and Macrocephaly;
OMIM:606053 Intellectual Developmental Disorder with Autism and Speech Delay;
OMIM:618906 Intellectual Developmental Disorder with Autistic Features and Language Delay, with or without Seizures; IDDALDS
OMIM:618725 Intellectual Developmental Disorder with Behavioral Abnormalities and Craniofacial Dysmorphism with or without Seizures; IDDBCS
OMIM:618316 Intellectual Developmental Disorder with Cardiac Defects and Dysmorphic Facies; IDDCDF
OMIM:618089 Intellectual Developmental Disorder with Dysmorphic Facies and Behavioral Abnormalities; IDDFBA
OMIM:617333 Intellectual Developmental Disorder with Dysmorphic Facies and Ptosis; IDDDFP
OMIM:617452 Intellectual Developmental Disorder with Dysmorphic Facies, Seizures, and Distal Limb Anomalies; IDDFSDA
OMIM:619031 Intellectual Developmental Disorder with Epilepsy, Behavioral Abnormalities, and Coarse Facies; IDDEBF
OMIM:618147 Intellectual Developmental Disorder with Hypertelorism and Distinctive Facies; IDDHDF
OMIM:618748 Intellectual Developmental Disorder with Hypotonia and Behavioral Abnormalities; IDDHBA
OMIM:619556 Intellectual Developmental Disorder with Hypotonia, Impaired Speech, and Dysmorphic Facies; IDDHISD
OMIM:618653 Intellectual Developmental Disorder with Impaired Language and Dysmorphic Facies; IDDILF
OMIM:609438 Intellectual Developmental Disorder with Keratoconus, Febrile Seizures, and Sinoatrial Block
OMIM:619911 Intellectual Developmental Disorder with Language Impairment and Early-Onset Dopa-Responsive Dystonia-Parkinsonism; IDLDP
OMIM:613670 Intellectual Developmental Disorder with Language Impairment and with or without Autistic Features; IDDLA
OMIM:618158 Intellectual Developmental Disorder with Macrocephaly, Seizures, and Speech Delay; IDDMSSD
OMIM:300749 Intellectual Developmental Disorder with Microcephaly and Pontine and Cerebellar Hypoplasia; MICPCH
OMIM:615866 Intellectual Developmental Disorder with Microcephaly and with or without Ocular Malformations or Hypogonadotropic Hypogonadism; IDDMOH
OMIM:620007 Intellectual Developmental Disorder with Muscle Tone Abnormalities and Distal Skeletal Defects; IDDMDS
OMIM:618608 Intellectual Developmental Disorder with Nasal Speech, Dysmorphic Facies, and Variable Skeletal Anomalies; IDNADFS
OMIM:617532 Intellectual Developmental Disorder with Neuropsychiatric Features;
OMIM:620086 Intellectual Developmental Disorder with Ocular Anomalies and Distinctive Facial Features; IDDOF
OMIM:609037 Intellectual Developmental Disorder with Optic Atrophy, Facial Dysmorphism, Microcephaly, and Short Stature
OMIM:618060 Intellectual Developmental Disorder with or without Epilepsy or Cerebellar Ataxia; IDDECA
OMIM:619844 Intellectual Developmental Disorder with or without Peripheral Neuropathy; IDDPN
OMIM:619150 Intellectual Developmental Disorder with Paroxysmal Dyskinesia or Seizures; IDDPADS
OMIM:617101 Intellectual Developmental Disorder with Persistence of Fetal Hemoglobin
OMIM:618808 Intellectual Developmental Disorder with Poor Growth and with or without Seizures or Ataxia; IDPOGSA
OMIM:619000 Intellectual Developmental Disorder with Seizures and Language Delay;
OMIM:618470 Intellectual Developmental Disorder with Severe Speech and Ambulation Defects; IDDSSAD
OMIM:618687 Intellectual Developmental Disorder with Short Stature and Behavioral Abnormalities; IDDSSBA
OMIM:618453 Intellectual Developmental Disorder with Short Stature and Variable Skeletal Anomalies; IDDSSA
OMIM:606220 Intellectual Developmental Disorder with Short Stature, Facial Anomalies, and Speech Defects; IDDSFAS
OMIM:602685 Intellectual Developmental Disorder with Spasticity and Pigmentary Tapetoretinal Degeneration
OMIM:619099 Intellectual Developmental Disorder with Speech Delay and Axonal Peripheral Neuropathy; IDDSAPN
OMIM:618506 Intellectual Developmental Disorder with Speech Delay and Dysmorphic Facies; IDDSDF
OMIM:618672 Intellectual Developmental Disorder with Speech Delay, Autism, and Dysmorphic Facies; IDDSADF
OMIM:618092 Intellectual Developmental Disorder with Speech Delay, Dysmorphic Facies, and T-Cell Abnormalities; IDDSFTA
OMIM:300923 Intellectual Developmental Disorder, X-Linked 100; XLID100
OMIM:300928 Intellectual Developmental Disorder, X-Linked 101; XLID101
OMIM:300982 Intellectual Developmental Disorder, X-Linked 103; XLID103
OMIM:300983 Intellectual Developmental Disorder, X-Linked 104; XLID104
OMIM:300984 Intellectual Developmental Disorder, X-Linked 105; XLID105
OMIM:300997 Intellectual Developmental Disorder, X-Linked 106; XLID106
OMIM:301013 Intellectual Developmental Disorder, X-Linked 107; XLID107
OMIM:301024 Intellectual Developmental Disorder, X-Linked 108; MRX108
OMIM:309548 Intellectual Developmental Disorder, X-Linked 109; XLID109
OMIM:301095 Intellectual Developmental Disorder, X-Linked 110; XLID110
OMIM:301107 Intellectual Developmental Disorder, X-Linked 111; XLID111
OMIM:301111 Intellectual Developmental Disorder, X-Linked 112; XLID112
OMIM:301116 Intellectual Developmental Disorder, X-Linked 113; XLID113
OMIM:301134 Intellectual Developmental Disorder, X-Linked 114; XLID114
OMIM:300062 Intellectual Developmental Disorder, X-Linked 14; XLID14
OMIM:300844 Intellectual Developmental Disorder, X-Linked 19; XLID19
OMIM:309530 Intellectual Developmental Disorder, X-Linked 1; XLID1
OMIM:300047 Intellectual Developmental Disorder, X-Linked 20; XLID20
OMIM:300143 Intellectual Developmental Disorder, X-Linked 21; XLID21
OMIM:300046 Intellectual Developmental Disorder, X-Linked 23; XLID23
OMIM:300419 Intellectual Developmental Disorder, X-Linked 29; XLID29
OMIM:300428 Intellectual Developmental Disorder, X-Linked 2; XLID2
OMIM:300558 Intellectual Developmental Disorder, X-Linked 30; XLID30
OMIM:300849 Intellectual Developmental Disorder, X-Linked 41; XLID41
OMIM:300372 Intellectual Developmental Disorder, X-Linked 42; XLID42
OMIM:300498 Intellectual Developmental Disorder, X-Linked 45; XLID45
OMIM:300436 Intellectual Developmental Disorder, X-Linked 46; XLID46
OMIM:300115 Intellectual Developmental Disorder, X-Linked 50; XLID50
OMIM:300324 Intellectual Developmental Disorder, X-Linked 53; XLID53
OMIM:300210 Intellectual Developmental Disorder, X-Linked 58; XLID58
OMIM:300387 Intellectual Developmental Disorder, X-Linked 63; XLID63
OMIM:300271 Intellectual Developmental Disorder, X-Linked 72; XLID72
OMIM:300355 Intellectual Developmental Disorder, X-Linked 73; XLID73
OMIM:300454 Intellectual Developmental Disorder, X-Linked 77; XLID77
OMIM:300433 Intellectual Developmental Disorder, X-Linked 81; XLID81
OMIM:300518 Intellectual Developmental Disorder, X-Linked 82; XLID82
OMIM:300505 Intellectual Developmental Disorder, X-Linked 84; XLID84
OMIM:300852 Intellectual Developmental Disorder, X-Linked 88; XLID88
OMIM:300848 Intellectual Developmental Disorder, X-Linked 89; XLID89
OMIM:300850 Intellectual Developmental Disorder, X-Linked 90; XLID90
OMIM:300577 Intellectual Developmental Disorder, X-Linked 91; XLID91
OMIM:300851 Intellectual Developmental Disorder, X-Linked 92; XLID92
OMIM:300659 Intellectual Developmental Disorder, X-Linked 93; XLID93
OMIM:300716 Intellectual Developmental Disorder, X-Linked 95; XLID95
OMIM:300802 Intellectual Developmental Disorder, X-Linked 96; XLID96
OMIM:300803 Intellectual Developmental Disorder, X-Linked 97; XLID97
OMIM:300912 Intellectual Developmental Disorder, X-Linked 98; XLID98
OMIM:300968 Intellectual Developmental Disorder, X-Linked 99, Syndromic, Female-Restricted; MRXS99F
OMIM:300919 Intellectual Developmental Disorder, X-Linked 99; XLID99
OMIM:309549 Intellectual Developmental Disorder, X-Linked 9; XLID9
OMIM:309545 Intellectual Developmental Disorder, X-Linked, Syndromic 12; MRXS12
OMIM:300055 Intellectual Developmental Disorder, X-Linked, Syndromic 13; MRXS13
OMIM:300676 Intellectual Developmental Disorder, X-Linked, Syndromic 14; MRXS14
OMIM:300858 Intellectual Developmental Disorder, X-Linked, Syndromic 17; MRXS17
OMIM:300886 Intellectual Developmental Disorder, X-Linked, Syndromic 32; MRXS32
OMIM:300966 Intellectual Developmental Disorder, X-Linked, Syndromic 33; MRXS33
OMIM:300967 Intellectual Developmental Disorder, X-Linked, Syndromic 34; MRXS34
OMIM:300998 Intellectual Developmental Disorder, X-Linked, Syndromic 35; MRXS35
OMIM:301118 Intellectual Developmental Disorder, X-Linked, Syndromic 37; MRXS37
OMIM:300218 Intellectual Developmental Disorder, X-Linked, Syndromic 7; MRXS7
OMIM:300709 Intellectual Developmental Disorder, X-Linked, Syndromic 9; MRXS9
OMIM:300262 Intellectual Developmental Disorder, X-Linked, Syndromic, Abidi Type;
OMIM:300261 Intellectual Developmental Disorder, X-Linked, Syndromic, Armfield Type; MRXSA
OMIM:300986 Intellectual Developmental Disorder, X-Linked, Syndromic, Bain Type;
OMIM:300486 Intellectual Developmental Disorder, X-Linked, Syndromic, Billuart Type; MRXSBL
OMIM:300354 Intellectual Developmental Disorder, X-Linked, Syndromic, Cabezas Type; MRXSC
OMIM:300243 Intellectual Developmental Disorder, X-Linked, Syndromic, Christianson Type; MRXSCH
OMIM:300861 Intellectual Developmental Disorder, X-Linked, Syndromic, Chudley-Schwartz Type; MRXSCS
OMIM:300534 Intellectual Developmental Disorder, X-Linked, Syndromic, Claes-Jensen Type; MRXSCJ
OMIM:309555 Intellectual Developmental Disorder, X-Linked, Syndromic, Gustavson Type; MRXSG
OMIM:301039 Intellectual Developmental Disorder, X-Linked, Syndromic, Hackmann-Di Donato Type; MRXSHD
OMIM:300423 Intellectual Developmental Disorder, X-Linked, Syndromic, Hedera Type; MRXSH
OMIM:301008 Intellectual Developmental Disorder, X-Linked, Syndromic, Houge Type;
OMIM:300957 Intellectual Developmental Disorder, X-Linked, Syndromic, Kumar Type;
OMIM:300260 Intellectual Developmental Disorder, X-Linked, Syndromic, Lubs Type;
OMIM:309520 Intellectual Developmental Disorder, X-Linked, Syndromic, Lujan-Fryns Type; MRXSLF
OMIM:300860 Intellectual Developmental Disorder, X-Linked, Syndromic, Nascimento Type; MRXSN
OMIM:301076 Intellectual Developmental Disorder, X-Linked, Syndromic, Pilorge Type; MRXSP
OMIM:300799 Intellectual Developmental Disorder, X-Linked, Syndromic, Raymond Type; MRXSR
OMIM:300238 Intellectual Developmental Disorder, X-Linked, Syndromic, Shashi Type; MRXSSH
OMIM:300263 Intellectual Developmental Disorder, X-Linked, Syndromic, Siderius Type; MRXSSD
OMIM:300958 Intellectual Developmental Disorder, X-Linked, Syndromic, Snijders Blok Type; MRXSSB
OMIM:309583 Intellectual Developmental Disorder, X-Linked, Syndromic, Snyder-Robinson Type; MRXSSR
OMIM:300434 Intellectual Developmental Disorder, X-Linked, Syndromic, Stocco Dos Santos Type; SDSX
OMIM:309590 Intellectual Developmental Disorder, X-Linked, Syndromic, Turner Type; MRXST
OMIM:309585 Intellectual Developmental Disorder, X-Linked, Syndromic, Wilson-Turner Type; WTS
OMIM:301066 Intellectual Developmental Disorder, X-Linked, Syndromic, with Pigmentary Mosaicism and Coarse Facies; MRXSPF
OMIM:300699 Intellectual Developmental Disorder, X-Linked, Syndromic, Wu Type;
OMIM:300123 Intellectual Developmental Disorder, X-Linked, with Panhypopituitarism
OMIM:203550 Intellectual Developmental Syndrome with Alopecia, Contractures, and Dwarfism
OMIM:619719 Intellectual Disability and Myopathy Syndrome; IDMYS
OMIM:309580 Intellectual Disability-Hypotonic Facies Syndrome, X-Linked, 1;
OMIM:147560 Interferon Antiviral Depressor
OMIM:243100 Internal Carotid Arteries, Hypoplasia of
OMIM:147820 Internal Carotid Artery, Spontaneous Dissection of
OMIM:615486 Interstitial Lung and Liver Disease; ILLD
OMIM:619611 Interstitial Lung Disease 1; ILD1
OMIM:178500 Interstitial Lung Disease 2; ILD2
OMIM:614817 Interstitial Nephritis, Karyomegalic; KMIN
OMIM:263000 Interstitial Pneumonitis, Desquamative, Familial; DIP
OMIM:603932 Intervertebral Disc Disease; IDD
OMIM:620045 Intestinal Dysmotility Syndrome; IDMTS
OMIM:300048 Intestinal Pseudoobstruction, Neuronal, Chronic Idiopathic, X-Linked;
OMIM:243185 Intestinal Pseudoobstruction with Patent Ductus Arteriosus and Natal Teeth
OMIM:243200 Intracranial Hypertension, Idiopathic
OMIM:614732 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies; IMAGE
OMIM:618336 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, Genital Anomalies, and Immunodeficiency; IMAGEI
OMIM:600546 Intrauterine Growth Retardation with Increased Mitomycin C Sensitivity
OMIM:243320 Intrinsic Factor and R Binder, Combined Congenital Deficiency of
OMIM:261000 Intrinsic Factor Deficiency; IFD
OMIM:147710 Intussusception
OMIM:609515 Iridogoniodysgenesis and Skeletal Anomalies
OMIM:308500 Iris Hypoplasia with Glaucoma; IHG
OMIM:610744 Iris Pattern
OMIM:601616 Iris Pigment Epithelium Anomalies
OMIM:147610 Iris Pigment Layer, Cleavage of
OMIM:601195 Iron Overload in Africa
OMIM:620121 Iron Overload, Susceptibility To; IO
OMIM:206200 Iron-Refractory Iron Deficiency Anemia; IRIDA
OMIM:147891 Ischiocoxopodopatellar Syndrome with or without Pulmonary Arterial Hypertension; ICPPS
OMIM:611283 Isobutyryl-Coa Dehydrogenase Deficiency; IBDD
OMIM:262400 Isolated Growth Hormone Deficiency, Type IA; IGHD1A
OMIM:612781 Isolated Growth Hormone Deficiency, Type IB; IGHD1B
OMIM:173100 Isolated Growth Hormone Deficiency, Type II; IGHD2
OMIM:307200 Isolated Growth Hormone Deficiency, Type III, with Agammaglobulinemia; IGHD3
OMIM:618157 Isolated Growth Hormone Deficiency, Type IV; IGHD4
OMIM:600801 Isoproterenol-Mediated Vasodilatation
OMIM:243440 Isotretinoin Embryopathy-Like Syndrome
OMIM:243500 Isovaleric Acidemia; IVA
OMIM:243450 Isovaleric Acid, Inability to Smell
OMIM:147750 Ivic Syndrome; IVIC
Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support. 		last database update
11/12/2024
MGI 6.24 		The Jackson Laboratory