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

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Human Diseases/Syndromes Beginning with "B"

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OMIM ID	Human Disease
OMIM:605838	Baby Rattle Pelvis Dysplasia
OMIM:619075	Bachmann-Bupp Syndrome; BABS
OMIM:614382	Bacteremia, Susceptibility to, 1; BACTS1
OMIM:614383	Bacteremia, Susceptibility to, 2; BACTS2
OMIM:606174	Baculum, Congenital Absence of
OMIM:615485	Bainbridge-Ropers Syndrome; BRPS
OMIM:618218	Baker-Gordon Syndrome; BAGOS
OMIM:218600	Baller-Gerold Syndrome; BGS
OMIM:241850	Bamforth-Lazarus Syndrome; BAMLAZ
OMIM:600348	Band Heterotopia; BH
OMIM:210740	Bangstad Syndrome
OMIM:109300	Banki Syndrome
OMIM:243310	Baraitser-Winter Syndrome 1; BRWS1
OMIM:614583	Baraitser-Winter Syndrome 2; BRWS2
OMIM:619255	Baralle-Macken Syndrome; BARMACS
OMIM:209885	Barber-Say Syndrome; BBRSAY
OMIM:615987	Bardet-Biedl Syndrome 10; BBS10
OMIM:615988	Bardet-Biedl Syndrome 11; BBS11
OMIM:615989	Bardet-Biedl Syndrome 12; BBS12
OMIM:615990	Bardet-Biedl Syndrome 13; BBS13
OMIM:615991	Bardet-Biedl Syndrome 14; BBS14
OMIM:615992	Bardet-Biedl Syndrome 15; BBS15
OMIM:615993	Bardet-Biedl Syndrome 16; BBS16
OMIM:615994	Bardet-Biedl Syndrome 17; BBS17
OMIM:615995	Bardet-Biedl Syndrome 18; BBS18
OMIM:615996	Bardet-Biedl Syndrome 19; BBS19
OMIM:209900	Bardet-Biedl Syndrome 1; BBS1
OMIM:619471	Bardet-Biedl Syndrome 20; BBS20
OMIM:617406	Bardet-Biedl Syndrome 21; BBS21
OMIM:617119	Bardet-Biedl Syndrome 22; BBS22
OMIM:615981	Bardet-Biedl Syndrome 2; BBS2
OMIM:600151	Bardet-Biedl Syndrome 3; BBS3
OMIM:615982	Bardet-Biedl Syndrome 4; BBS4
OMIM:615983	Bardet-Biedl Syndrome 5; BBS5
OMIM:605231	Bardet-Biedl Syndrome 6; BBS6
OMIM:615984	Bardet-Biedl Syndrome 7; BBS7
OMIM:615985	Bardet-Biedl Syndrome 8; BBS8
OMIM:615986	Bardet-Biedl Syndrome 9; BBS9
OMIM:614266	Barrett Esophagus
OMIM:302060	Barth Syndrome; BTHS
OMIM:149200	Bart-Pumphrey Syndrome; BAPS
OMIM:263650	Bartsocas-Papas Syndrome 1; BPS1
OMIM:619339	Bartsocas-Papas Syndrome 2; BPS2
OMIM:601678	Bartter Syndrome, Type 1, Antenatal; BARTS1
OMIM:241200	Bartter Syndrome, Type 2, Antenatal; BARTS2
OMIM:607364	Bartter Syndrome, Type 3; BARTS3
OMIM:602522	Bartter Syndrome, Type 4a, Neonatal, with Sensorineural Deafness;
OMIM:613090	Bartter Syndrome, Type 4b, Neonatal, with Sensorineural Deafness;
OMIM:300971	Bartter Syndrome, Type 5, Antenatal, Transient; BARTS5
OMIM:604451	Basal Cell Carcinoma, Infundibulocystic
OMIM:605462	Basal Cell Carcinoma, Susceptibility to, 1; BCC1
OMIM:613058	Basal Cell Carcinoma, Susceptibility to, 2; BCC2
OMIM:613059	Basal Cell Carcinoma, Susceptibility to, 3; BCC3
OMIM:613061	Basal Cell Carcinoma, Susceptibility to, 4; BCC4
OMIM:613062	Basal Cell Carcinoma, Susceptibility to, 5; BCC5
OMIM:613063	Basal Cell Carcinoma, Susceptibility to, 6; BCC6
OMIM:614740	Basal Cell Carcinoma, Susceptibility to, 7; BCC7
OMIM:109400	Basal Cell Nevus Syndrome 1; BCNS1
OMIM:620343	Basal Cell Nevus Syndrome 2; BCNS2
OMIM:213600	Basal Ganglia Calcification, Idiopathic, 1; IBGC1
OMIM:615007	Basal Ganglia Calcification, Idiopathic, 4; IBGC4
OMIM:615483	Basal Ganglia Calcification, Idiopathic, 5; IBGC5
OMIM:616413	Basal Ganglia Calcification, Idiopathic, 6; IBGC6
OMIM:618317	Basal Ganglia Calcification, Idiopathic, 7, Autosomal Recessive;
OMIM:618824	Basal Ganglia Calcification, Idiopathic, 8, Autosomal Recessive;
OMIM:620786	Basal Ganglia Calcification, Idiopathic, 9, Autosomal Recessive;
OMIM:114100	Basal Ganglia Calcification, Idiopathic, Childhood-Onset
OMIM:607483	Basal Ganglia Disease, Biotin-Thiamine Responsive; BTBGD
OMIM:126700	Basal Laminar Drusen
OMIM:605827	Basaloid Follicular Hamartoma Syndrome, Generalized, Autosomal Dominant;
OMIM:129200	Basan Syndrome
OMIM:616449	Basel-Vanagaite-Smirin-Yosef Syndrome; BVSYS
OMIM:603738	Basic Transcription Factor 3 Pseudogene 12; BTF3P12
OMIM:603739	Basic Transcription Factor 3 Pseudogene 13; BTF3P13
OMIM:109500	Basilar Impression, Primary
OMIM:301032	Basilicata-Akhtar Syndrome; MRXSBA
OMIM:255300	Batten-Turner Congenital Myopathy
OMIM:301845	Bazex-Dupre-Christol Syndrome; BDCS
OMIM:612394	Bcard Syndrome; BCARD
OMIM:151430	B-Cell Cll/Lymphoma 2; BCL2
OMIM:616452	B-Cell Expansion with NFKB and T-Cell Anergy; BENT
OMIM:109540	B-Cell Growth Factor; BCGF
OMIM:609296	B-Cell Immunodeficiency, Distal Limb Anomalies, and Urogenital Malformations; BILU
OMIM:619326	Bdv Syndrome; BDVS
OMIM:123790	Beare-Stevenson Cutis Gyrata Syndrome; BSTVS
OMIM:613680	Beaulieu-Boycott-Innes Syndrome; BBIS
OMIM:604919	Becker Nevus Syndrome; BNS
OMIM:618798	Beck-Fahrner Syndrome; BEFAHRS
OMIM:130650	Beckwith-Wiedemann Syndrome; BWS
OMIM:209970	Beemer Lethal Malformation Syndrome
OMIM:109650	Behcet Syndrome
OMIM:210000	Behr Syndrome; BEHRS
OMIM:614592	Bent Bone Dysplasia Syndrome 1; BBDS1
OMIM:620076	Bent Bone Dysplasia Syndrome 2; BBDS2
OMIM:231200	Bernard-Soulier Syndrome; BSS
OMIM:153670	Bernard-Soulier Syndrome, Type A2, Autosomal Dominant; BSSA2
OMIM:210050	Berry Aneurysm, Cirrhosis, Pulmonary Emphysema, and Cerebral Calcification
OMIM:611809	Bestrophinopathy, Autosomal Recessive; ARB
OMIM:109690	Beta-2-Adrenergic Receptor; ADRB2
OMIM:109660	Beta-Amino Acids, Renal Transport Of; AABT
OMIM:210100	Beta-Aminoisobutyric Aciduria; BAIBA
OMIM:617956	Beta-Glucopyranoside Tasting; BGLPT
OMIM:109640	Beta-Glycerol Phosphatase; GPB
OMIM:613985	Beta-Thalassemia
OMIM:603902	Beta-Thalassemia, Dominant Inclusion Body Type
OMIM:613161	Beta-Ureidopropionase Deficiency; UPB1D
OMIM:158810	Bethlem Myopathy 1A; BTHLM1A
OMIM:620725	Bethlem Myopathy 1B; BTHLM1B
OMIM:620726	Bethlem Myopathy 1C; BTHLM1C
OMIM:616471	Bethlem Myopathy 2; BTHLM2
OMIM:142669	Beukes Hip Dysplasia; HDB
OMIM:210350	Biemond Syndrome II
OMIM:210370	Bietti Crystalline Corneoretinal Dystrophy; BCD
OMIM:109740	Bifid Nose, Autosomal Dominant
OMIM:210400	Bifid Nose, Autosomal Recessive
OMIM:608980	Bifid Nose with or without Anorectal and Renal Anomalies; BNAR
OMIM:619232	Bile Acid Conjugation Defect 1; BACD1
OMIM:613291	Bile Acid Malabsorption, Primary, 1; PBAM1
OMIM:619481	Bile Acid Malabsorption, Primary, 2; PBAM2
OMIM:607765	Bile Acid Synthesis Defect, Congenital, 1; CBAS1
OMIM:235555	Bile Acid Synthesis Defect, Congenital, 2; CBAS2
OMIM:613812	Bile Acid Synthesis Defect, Congenital, 3; CBAS3
OMIM:214950	Bile Acid Synthesis Defect, Congenital, 4; CBAS4
OMIM:616278	Bile Acid Synthesis Defect, Congenital, 5; CBAS5
OMIM:617308	Bile Acid Synthesis Defect, Congenital, 6; CBAS6
OMIM:608063	Bile and Pancreatic Ducts, Complete Absence of
OMIM:603003	Bile Duct Cysts
OMIM:210500	Biliary Atresia, Extrahepatic; EHBA
OMIM:109720	Biliary Cirrhosis, Primary, 1; PBC1
OMIM:613007	Biliary Cirrhosis, Primary, 2; PBC2
OMIM:613008	Biliary Cirrhosis, Primary, 3; PBC3
OMIM:614220	Biliary Cirrhosis, Primary, 4; PBC4
OMIM:614221	Biliary Cirrhosis, Primary, 5; PBC5
OMIM:210550	Biliary Malformation with Renal Tubular Insufficiency
OMIM:619534	Biliary, Renal, Neurologic, and Skeletal Syndrome; BRENS
OMIM:253260	Biotinidase Deficiency
OMIM:618256	Biparental Mitochondrial DNA Transmission
OMIM:613393	Birbeck Granule Deficiency
OMIM:605808	Birdshot Chorioretinopathy
OMIM:620071	Birk-Aharoni Syndrome; BKAH
OMIM:612292	Birk-Barel Syndrome; BIBARS
OMIM:617595	Birk-Landau-Perez Syndrome; BILAPES
OMIM:135150	Birt-Hogg-Dube Syndrome 1; BHD1
OMIM:620459	Birt-Hogg-Dube Syndrome 2; BHD2
OMIM:262000	Bjornstad Syndrome; BJS
OMIM:109780	Bkm DNA
OMIM:109800	Bladder Cancer
OMIM:109820	Bladder Diverticulum
OMIM:191800	Bladder Dysfunction, Autonomic, with Impaired Pupillary Reflex and Secondary Cakut; BAIPRCK
OMIM:600057	Bladder Exstrophy and Epispadias Complex; BEEC
OMIM:186580	Blau Syndrome; BLAUS
OMIM:605913	Bleeding Disorder, East Texas Type
OMIM:614201	Bleeding Disorder, Platelet-Type, 11; BDPLT11
OMIM:605735	Bleeding Disorder, Platelet-Type, 12; BDPLT12
OMIM:614009	Bleeding Disorder, Platelet-Type, 13, Susceptibility To; BDPLT13
OMIM:614158	Bleeding Disorder, Platelet-Type, 14; BDPLT14
OMIM:615193	Bleeding Disorder, Platelet-Type, 15; BDPLT15
OMIM:187800	Bleeding Disorder, Platelet-Type, 16; BDPLT16
OMIM:187900	Bleeding Disorder, Platelet-Type, 17; BDPLT17
OMIM:615888	Bleeding Disorder, Platelet-Type, 18; BDPLT18
OMIM:616176	Bleeding Disorder, Platelet-Type, 19; BDPLT19
OMIM:616913	Bleeding Disorder, Platelet-Type, 20; BDPLT20
OMIM:617443	Bleeding Disorder, Platelet-Type, 21; BDPLT21
OMIM:618462	Bleeding Disorder, Platelet-Type, 22; BDPLT22
OMIM:619271	Bleeding Disorder, Platelet-Type, 24; BDPLT24
OMIM:620486	Bleeding Disorder, Platelet-Type, 25; BDPLT25
OMIM:609821	Bleeding Disorder, Platelet-Type, 8; BDPLT8
OMIM:614200	Bleeding Disorder, Platelet-Type, 9; BDPLT9
OMIM:620715	Bleeding Disorder, Vascular-Type; BDVAS
OMIM:109900	Blepharochalasis and Double Lip
OMIM:110000	Blepharochalasis, Superior
OMIM:119580	Blepharocheilodontic Syndrome 1; BCDS1
OMIM:617681	Blepharocheilodontic Syndrome 2; BCDS2
OMIM:110050	Blepharonasofacial Malformation Syndrome
OMIM:619293	Blepharophimosis-Impaired Intellectual Development Syndrome; BIS
OMIM:110100	Blepharophimosis, Ptosis, and Epicanthus Inversus; BPES
OMIM:604314	Blepharophimosis with Facial and Genital Anomalies and Impaired Intellectual Development
OMIM:210745	Blepharophimosis with Ptosis, Syndactyly, and Short Stature
OMIM:110150	Blepharoptosis, Myopia, and Ectopia Lentis
OMIM:606798	Blepharospasm, Benign Essential, Susceptibility to
OMIM:619226	Blistering, Acantholytic, of Oral and Laryngeal Mucosa; ABOLM
OMIM:620975	Blood Group, Anton System
OMIM:619812	Blood Group, Emm System; EMM
OMIM:620207	Blood Group, Er; ER
OMIM:618983	Blood Group, Lewis System; LE
OMIM:615018	Blood Group, Sid System; SID
OMIM:210900	Bloom Syndrome; BLM
OMIM:259200	Blount Disease, Adolescent
OMIM:188700	Blount Disease, Infantile
OMIM:303700	Blue Cone Monochromacy; BCM
OMIM:211000	Blue Diaper Syndrome
OMIM:603670	Blue Nevi, Familial Multiple
OMIM:112200	Blue Rubber Bleb Nevus
OMIM:300054	Body Length, Mouse, Human Homolog
OMIM:617885	Body Mass Index Quantitative Trait Locus 19; BMIQ19
OMIM:618406	Body Mass Index Quantitative Trait Locus 20; BMIQ20
OMIM:605039	Bohring-Opitz Syndrome; BOPS
OMIM:616754	Bombay Phenotype
OMIM:211120	Bone Dysplasia, Lethal, Holmgren Type
OMIM:620044	Bone Marrow Failure and Diabetes Mellitus Syndrome; BMFDMS
OMIM:614675	Bone Marrow Failure Syndrome 1; BMFS1
OMIM:615715	Bone Marrow Failure Syndrome 2; BMFS2
OMIM:617052	Bone Marrow Failure Syndrome 3; BMFS3
OMIM:618116	Bone Marrow Failure Syndrome 4; BMFS4
OMIM:618165	Bone Marrow Failure Syndrome 5; BMFS5
OMIM:618849	Bone Marrow Failure Syndrome 6; BMFS6
OMIM:112270	Bone Pain, Periodic
OMIM:112300	Book Syndrome
OMIM:112310	Boomerang Dysplasia; BOOMD
OMIM:301900	Borjeson-Forssman-Lehmann Syndrome; BFLS
OMIM:300843	Bornholm Eye Disease; BED
OMIM:615722	Bosch-Boonstra-Schaaf Optic Atrophy Syndrome; BBSOAS
OMIM:603457	Bosma Arhinia Microphthalmia Syndrome; BAMS
OMIM:607475	Bothnia Retinal Dystrophy
OMIM:215470	Boucher-Neuhauser Syndrome; BNHS
OMIM:619543	Boudin-Mortier Syndrome; BOMOS
OMIM:211180	Bowen-Conradi Syndrome; BWCNS
OMIM:211200	Bowen Syndrome of Multiple Malformations
OMIM:211355	Bowing of Long Bones, Asymmetric and Symmetric
OMIM:601357	Brachial Amelia, Cleft Lip, and Holoprosencephaly; ACLH
OMIM:608585	Brachial Palsy, Familial Congenital
OMIM:112370	Brachmann-De Lange-Like Facial Changes with Microcephaly, Metatarsus Adductus, and Developmental Delay
OMIM:601353	Brachycephaly, Deafness, Cataract, Microstomia, and Impaired Intellectual Development
OMIM:617412	Brachycephaly, Trichomegaly, and Developmental Delay; BTDD
OMIM:610023	Brachydactyly, Coloboma, and Anterior Segment Dysgenesis
OMIM:112440	Brachydactyly, Combined B and E Types
OMIM:113450	Brachydactyly-Distal Symphalangism Syndrome
OMIM:113310	Brachydactyly-Ectrodactyly with Fibular Aplasia or Hypoplasia
OMIM:602561	Brachydactyly, Intraventricular Septal Defect, and Deafness
OMIM:301940	Brachydactyly, Mononen Type
OMIM:113400	Brachydactyly-Nystagmus-Cerebellar Ataxia
OMIM:112450	Brachydactyly, Preaxial, with Hallux Varus and Thumb Abduction
OMIM:610713	Brachydactyly-Syndactyly Syndrome; BDSD
OMIM:607004	Brachydactyly, Type A1, B; BDA1B
OMIM:112500	Brachydactyly, Type A1; BDA1
OMIM:615072	Brachydactyly, Type A1, C; BDA1C
OMIM:616849	Brachydactyly, Type A1, D; BDA1D
OMIM:112600	Brachydactyly, Type A2; BDA2
OMIM:211369	Brachydactyly, Type A2, with Microcephaly
OMIM:112700	Brachydactyly, Type A3; BDA3
OMIM:112800	Brachydactyly, Type A4; BDA4
OMIM:113000	Brachydactyly, Type B1; BDB1
OMIM:611377	Brachydactyly, Type B2; BDB2
OMIM:113100	Brachydactyly, Type C; BDC
OMIM:113200	Brachydactyly, Type D; BDD
OMIM:113300	Brachydactyly, Type E1; BDE1
OMIM:613382	Brachydactyly, Type E2; BDE2
OMIM:113301	Brachydactyly, Type E, with Atrial Septal Defect, Type II
OMIM:113470	Brachymesomelia-Renal Syndrome
OMIM:211370	Brachymetapody-Anodontia-Hypotrichosis-Albinoidism
OMIM:113475	Brachymetatarsus IV
OMIM:113477	Brachymorphism-Onychodysplasia-Dysphalangism Syndrome
OMIM:271530	Brachyolmia Type 1, Hobaek Type; BCYM1A
OMIM:271630	Brachyolmia Type 1, Toledo Type; BCYM1B
OMIM:613678	Brachyolmia Type 2; BCYM2
OMIM:113500	Brachyolmia Type 3; BCYM3
OMIM:612847	Brachyolmia Type 4 with Mild Epiphyseal and Metaphyseal Changes;
OMIM:609945	Brachyphalangy, Polydactyly, and Tibial Aplasia/Hypoplasia
OMIM:113480	Brachytelephalangy with Characteristic Facies and Kallmann Syndrome
OMIM:619980	Braddock-Carey Syndrome 1; BRDCS1
OMIM:619981	Braddock-Carey Syndrome 2; BRDCS2
OMIM:618476	Brain Abnormalities, Neurodegeneration, and Dysosteosclerosis;
OMIM:620943	Brain Malformation Renal Syndrome; BMRS
OMIM:613735	Brain Malformations with or without Urinary Tract Defects; BRMUTD
OMIM:175780	Brain Small Vessel Disease 1 with or without Ocular Anomalies; BSVD1
OMIM:614483	Brain Small Vessel Disease 2; BSVD2
OMIM:618360	Brain Small Vessel Disease 3; BSVD3
OMIM:614923	Branched-Chain Keto Acid Dehydrogenase Kinase Deficiency; BCKDKD
OMIM:620186	Branchial Arch Abnormalities, Choanal Atresia, Athelia, Hearing Loss, and Hypothyroidism Syndrome; BCAHH
OMIM:301950	Branchial Arch Syndrome, X-Linked
OMIM:113600	Branchial Cleft Anomalies
OMIM:113610	Branchial Myoclonus with Spastic Paraparesis and Cerebellar Ataxia
OMIM:609166	Branchiogenic-Deafness Syndrome
OMIM:113620	Branchiooculofacial Syndrome; BOFS
OMIM:602588	Branchiootic Syndrome 1; BOS1
OMIM:120502	Branchiootic Syndrome 2; BOS2
OMIM:608389	Branchiootic Syndrome 3; BOS3
OMIM:113650	Branchiootorenal Syndrome 1; BOR1
OMIM:610896	Branchiootorenal Syndrome 2; BOR2
OMIM:114480	Breast Cancer
OMIM:113721	Breast Cancer-Related Regulator of Tp53
OMIM:604370	Breast-Ovarian Cancer, Familial, Susceptibility to, 1; BROVCA1
OMIM:612555	Breast-Ovarian Cancer, Familial, Susceptibility to, 2; BROVCA2
OMIM:613399	Breast-Ovarian Cancer, Familial, Susceptibility to, 3; BROVCA3
OMIM:614291	Breast-Ovarian Cancer, Familial, Susceptibility to, 4; BROVCA4
OMIM:620442	Breast-Ovarian Cancer, Familial, Susceptibility to, 5; BROVCA5
OMIM:113700	Breasts and/or Nipples, Aplasia or Hypoplasia of, 1; BNAH1
OMIM:616001	Breasts and/or Nipples, Aplasia or Hypoplasia of, 2; BNAH2
OMIM:607578	Breath-Holding Spells
OMIM:603828	Brittle Bone Disorder
OMIM:229200	Brittle Cornea Syndrome 1; BCS1
OMIM:614170	Brittle Cornea Syndrome 2; BCS2
OMIM:602071	Broad Terminal Phalanges, Familial
OMIM:601003	Brody Disease; BROD
OMIM:620984	Bronchiectasis and Nasal Polyposis; BENP
OMIM:211400	Bronchiectasis with or without Elevated Sweat Chloride 1; BESC1
OMIM:613021	Bronchiectasis with or without Elevated Sweat Chloride 2; BESC2
OMIM:613071	Bronchiectasis with or without Elevated Sweat Chloride 3; BESC3
OMIM:605041	Brooke-Spiegler Syndrome; BRSS
OMIM:616407	Brown Syndrome; BRWNS
OMIM:211530	Brown-Vialetto-Van Laere Syndrome 1; BVVLS1
OMIM:614707	Brown-Vialetto-Van Laere Syndrome 2; BVVLS2
OMIM:259450	Bruck Syndrome 1; BRKS1
OMIM:609220	Bruck Syndrome 2; BRKS2
OMIM:601144	Brugada Syndrome 1; BRGDA1
OMIM:611777	Brugada Syndrome 2; BRGDA2
OMIM:611875	Brugada Syndrome 3; BRGDA3
OMIM:611876	Brugada Syndrome 4; BRGDA4
OMIM:612838	Brugada Syndrome 5; BRGDA5
OMIM:613119	Brugada Syndrome 6; BRGDA6
OMIM:613120	Brugada Syndrome 7; BRGDA7
OMIM:613123	Brugada Syndrome 8; BRGDA8
OMIM:616399	Brugada Syndrome 9; BRGDA9
OMIM:619690	Brunet-Wagner Neurodevelopmental Syndrome; BRUWAG
OMIM:300615	Brunner Syndrome; BRNRS
OMIM:619720	Bryant-Li-Bhoj Neurodevelopmental Syndrome 1; BRYLIB1
OMIM:619721	Bryant-Li-Bhoj Neurodevelopmental Syndrome 2; BRYLIB2
OMIM:600880	Budd-Chiari Syndrome; BDCHS
OMIM:211480	Buerger Disease
OMIM:607499	Bulimia Nervosa, Susceptibility To; BULN
OMIM:302000	Bullous Dystrophy, Hereditary Macular Type; HBDM
OMIM:113950	Bundle Branch Block, Familial Isolated Complete Right
OMIM:113955	Bungarotoxin, Alpha, Receptor For; BGTXR
OMIM:619314	Buratti-Harel Syndrome; BURHAS
OMIM:113970	Burkitt Lymphoma; BL
OMIM:608572	Burn-Mckeown Syndrome; BMKS
OMIM:610446	Buruli Ulcer, Susceptibility to
OMIM:166700	Buschke-Ollendorff Syndrome; BOS
OMIM:617936	Butyrylcholinesterase Deficiency; BCHED
OMIM:113960	Butyrylesterase 1

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