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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 "B"

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

OMIM IDHuman Disease
OMIM:605838 Baby Rattle Pelvis Dysplasia
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:218600 Baller-Gerold Syndrome; BGS
OMIM:600348 Band Heterotopia; BH
OMIM:251290 Band-Like Calcification with Simplified Gyration and Polymicrogyria;
OMIM:210740 Bangstad Syndrome
OMIM:109300 Banki Syndrome
OMIM:153480 Bannayan-Riley-Ruvalcaba Syndrome; BRRS
OMIM:243310 Baraitser-Winter Syndrome 1; BRWS1
OMIM:614583 Baraitser-Winter Syndrome 2; BRWS2
OMIM:300881 Baratela-Scott Syndrome
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:617119 Bardet-Biedl Syndrome 20; BBS20
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:604571 Bare Lymphocyte Syndrome, Type I
OMIM:209920 Bare Lymphocyte Syndrome, Type II
OMIM:614266 Barrett Esophagus
OMIM:302060 Barth Syndrome; BTHS
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; BCNS
OMIM:213600 Basal Ganglia Calcification, Idiopathic, 1; IBGC1
OMIM:606656 Basal Ganglia Calcification, Idiopathic, 2; IBGC2
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:114100 Basal Ganglia Calcification, Idiopathic, Childhood-Onset
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:109500 Basilar Impression, Primary
OMIM:301845 Bazex Syndrome; BZX
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
OMIM:123790 Beare-Stevenson Cutis Gyrata Syndrome; BSTVS
OMIM:613680 Beaulieu-Boycott-Innes Syndrome; BBIS
OMIM:604919 Becker Nevus Syndrome
OMIM:130650 Beckwith-Wiedemann Syndrome; BWS
OMIM:209970 Beemer Lethal Malformation Syndrome
OMIM:109650 Behcet Syndrome
OMIM:210000 Behr Syndrome; BEHRS
OMIM:169600 Benign Chronic Pemphigus; BCPM
OMIM:614592 Bent Bone Dysplasia Syndrome; BBDS
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:109630 Beta-1-Adrenergic Receptor; ADRB1
OMIM:109690 Beta-2-Adrenergic Receptor; ADRB2
OMIM:109660 Beta-Amino Acids, Renal Transport Of; AABT
OMIM:210100 Beta-Aminoisobutyric Acid, Urinary Excretion of
OMIM:613985 Beta-Thalassemia
OMIM:603902 Beta-Thalassemia, Dominant Inclusion Body Type
OMIM:613161 Beta-Ureidopropionase Deficiency; UPB1D
OMIM:158810 Bethlem Myopathy 1; BTHLM1
OMIM:616471 Bethlem Myopathy 2; BTHLM2
OMIM:142669 Beukes Hip Dysplasia; BHD
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:613291 Bile Acid Malabsorption, Primary; PBAM
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:253260 Biotinidase Deficiency
OMIM:613393 Birbeck Granule Deficiency
OMIM:605808 Birdshot Chorioretinopathy
OMIM:612292 Birk-Barel Mental Retardation Dysmorphism Syndrome
OMIM:135150 Birt-Hogg-Dube Syndrome; BHD
OMIM:222800 Bisphosphoglycerate Mutase Deficiency
OMIM:262000 Bjornstad Syndrome; BJS
OMIM:109800 Bladder Cancer
OMIM:109820 Bladder Diverticulum
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:609821 Bleeding Disorder, Platelet-Type, 8; BDPLT8
OMIM:614200 Bleeding Disorder, Platelet-Type, 9; BDPLT9
OMIM:109900 Blepharochalasis and Double Lip
OMIM:110000 Blepharochalasis, Superior
OMIM:119580 Blepharocheilodontic Syndrome; BCDS
OMIM:110050 Blepharonasofacial Malformation Syndrome
OMIM:110100 Blepharophimosis, Ptosis, and Epicanthus Inversus; BPES
OMIM:604314 Blepharophimosis with Facial and Genital Anomalies and Mental Retardation
OMIM:210745 Blepharophimosis with Ptosis, Syndactyly, and Short Stature
OMIM:110150 Blepharoptosis, Myopia, and Ectopia Lentis
OMIM:606798 Blepharospasm, Benign Essential
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:605039 Bohring-Opitz Syndrome; BOPS
OMIM:616754 Bombay Phenotype
OMIM:211120 Bone Dysplasia, Lethal, Holmgren Type
OMIM:612394 Bone Fragility with Contractures, Arterial Rupture, and Deafness
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:112270 Bone Pain, Periodic
OMIM:112300 Book Syndrome
OMIM:112310 Boomerang Dysplasia
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: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:211380 Brachioskeletogenital Syndrome
OMIM:112370 Brachmann-De Lange-Like Facial Changes with Microcephaly, Metatarsus Adductus, and Developmental Delay
OMIM:601353 Brachycephaly, Deafness, Cataract, Microstomia, and Mental Retardation
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:613627 Brachydactyly, Type A1, with Short Stature, Scoliosis, Microcephaly, Ptosis, Hearing Loss, and Mental Retardation
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:607595 Brain Small Vessel Disease with or without Ocular Anomalies; BSVD
OMIM:614923 Branched-Chain Keto Acid Dehydrogenase Kinase Deficiency; BCKDKD
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
OMIM:608389 Branchiootic Syndrome 3; BOS3
OMIM:113650 Branchiootorenal Syndrome 1; BOR1
OMIM:610896 Branchiootorenal Syndrome 2; BOR2
OMIM:114480 Breast Cancer
OMIM:600048 Breast Cancer, 11-22 Translocation-Associated; BRCATA
OMIM:605365 Breast Cancer 3; BRCA3
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: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 Myopathy
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:211450 Bronchomalacia
OMIM:605041 Brooke-Spiegler Syndrome; BRSS
OMIM:300612 Brooks-Wisniewski-Brown Syndrome
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:300615 Brunner Syndrome; BRNRS
OMIM:600880 Budd-Chiari Syndrome; BDCHS
OMIM:211480 Buerger Disease
OMIM:607499 Bulimia Nervosa, Susceptibility to, 1; BULN1
OMIM:610269 Bulimia Nervosa, Susceptibility to, 2; BULN2
OMIM:302000 Bullous Dystrophy, Hereditary Macular Type
OMIM:113950 Bundle Branch Block, Familial Isolated Complete Right
OMIM:113970 Burkitt Lymphoma; BL
OMIM:608572 Burn-Mckeown Syndrome; BMKS
OMIM:610446 Buruli Ulcer, Susceptibility to
OMIM:166700 Buschke-Ollendorff Syndrome; BOS
OMIM:177400 Butyrylcholinesterase; BCHE
OMIM:113960 Butyrylesterase 1

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last database update
03/21/2017
MGI 6.08
The Jackson Laboratory