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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
605838 Baby Rattle Pelvis Dysplasia
614382 Bacteremia, Susceptibility to, 1; BACTS1
614383 Bacteremia, Susceptibility to, 2; BACTS2
606174 Baculum, Congenital Absence of
615485 Bainbridge-Ropers Syndrome; BRPS
218600 Baller-Gerold Syndrome; BGS
600348 Band Heterotopia of Brain
251290 Band-Like Calcification with Simplified Gyration and Polymicrogyria;
210740 Bangstad Syndrome
109300 Banki Syndrome
153480 Bannayan-Riley-Ruvalcaba Syndrome; BRRS (3 mouse models)
243310 Baraitser-Winter Syndrome 1; BRWS1
614583 Baraitser-Winter Syndrome 2; BRWS2
300881 Baratela-Scott Syndrome
209885 Barber-Say Syndrome
209900 Bardet-Biedl Syndrome; BBS (10 mouse models)
604571 Bare Lymphocyte Syndrome, Type I
209920 Bare Lymphocyte Syndrome, Type II (2 mouse models)
614266 Barrett Esophagus (1 mouse models)
302060 Barth Syndrome; BTHS (4 mouse models)
601678 Bartter Syndrome, Antenatal, Type 1 (2 mouse models)
241200 Bartter Syndrome, Antenatal, Type 2 (1 mouse models)
607364 Bartter Syndrome, Type 3
602522 Bartter Syndrome, Type 4a (2 mouse models)
613090 Bartter Syndrome, Type 4b
604451 Basal Cell Carcinoma, Infundibulocystic
605462 Basal Cell Carcinoma, Susceptibility to, 1; BCC1 (1 mouse models)
613058 Basal Cell Carcinoma, Susceptibility to, 2; BCC2
613059 Basal Cell Carcinoma, Susceptibility to, 3; BCC3
613061 Basal Cell Carcinoma, Susceptibility to, 4; BCC4
613062 Basal Cell Carcinoma, Susceptibility to, 5; BCC5
613063 Basal Cell Carcinoma, Susceptibility to, 6; BCC6
614740 Basal Cell Carcinoma, Susceptibility to, 7; BCC7
109400 Basal Cell Nevus Syndrome; BCNS (4 mouse models)
213600 Basal Ganglia Calcification, Idiopathic, 1; IBGC1
606656 Basal Ganglia Calcification, Idiopathic, 2; IBGC2
615007 Basal Ganglia Calcification, Idiopathic, 4; IBGC4
615483 Basal Ganglia Calcification, Idiopathic, 5; IBGC5
114100 Basal Ganglia Calcification, Idiopathic, Childhood-Onset
126700 Basal Laminar Drusen
605827 Basaloid Follicular Hamartoma Syndrome, Generalized, Autosomal Dominant;
109500 Basilar Impression, Primary
301845 Bazex Syndrome; BZX
151430 B-Cell Cll/Lymphoma 2; BCL2
109540 B-Cell Growth Factor; BCGF
609296 B-Cell Immunodeficiency, Distal Limb Anomalies, and Urogenital Malformations
123790 Beare-Stevenson Cutis Gyrata Syndrome; BSTVS (1 mouse models)
613680 Beaulieu-Boycott-Innes Syndrome; BBIS
604919 Becker Nevus Syndrome
130650 Beckwith-Wiedemann Syndrome; BWS (3 mouse models)
209970 Beemer Lethal Malformation Syndrome
109600 Beeturia
109650 Behcet Syndrome
210000 Behr Syndrome
169600 Benign Chronic Pemphigus; BCPM
614592 Bent Bone Dysplasia Syndrome; BBDS
231200 Bernard-Soulier Syndrome; BSS (5 mouse models)
153670 Bernard-Soulier Syndrome, Type A2, Autosomal Dominant; BSSA2
210050 Berry Aneurysm, Cirrhosis, Pulmonary Emphysema, and Cerebral Calcification
611809 Bestrophinopathy, Autosomal Recessive; ARB (2 mouse models)
109630 Beta-1-Adrenergic Receptor; ADRB1
109690 Beta-2-Adrenergic Receptor; ADRB2
109660 Beta-Amino Acids, Renal Transport Of; AABT
210100 Beta-Aminoisobutyric Acid, Urinary Excretion of
250620 Beta-Hydroxyisobutyryl Coa Deacylase Deficiency
613985 Beta-Thalassemia (15 mouse models)
603902 Beta-Thalassemia, Dominant Inclusion Body Type
613161 Beta-Ureidopropionase Deficiency
158810 Bethlem Myopathy (1 mouse models)
210350 Biemond Syndrome II
210370 Bietti Crystalline Corneoretinal Dystrophy
109740 Bifid Nose, Autosomal Dominant
210400 Bifid Nose, Autosomal Recessive
608980 Bifid Nose with or without Anorectal and Renal Anomalies; BNAR
613291 Bile Acid Malabsorption, Primary; PBAM
607765 Bile Acid Synthesis Defect, Congenital, 1; CBAS1
235555 Bile Acid Synthesis Defect, Congenital, 2; CBAS2
613812 Bile Acid Synthesis Defect, Congenital, 3; CBAS3
214950 Bile Acid Synthesis Defect, Congenital, 4; CBAS4
608063 Bile and Pancreatic Ducts, Complete Absence of
603003 Bile Duct Cysts
210500 Biliary Atresia, Extrahepatic; EHBA
109720 Biliary Cirrhosis, Primary, 1; PBC1 (1 mouse models)
613007 Biliary Cirrhosis, Primary, 2; PBC2
613008 Biliary Cirrhosis, Primary, 3; PBC3
614220 Biliary Cirrhosis, Primary, 4; PBC4
614221 Biliary Cirrhosis, Primary, 5; PBC5
210550 Biliary Malformation with Renal Tubular Insufficiency
253260 Biotinidase Deficiency (1 mouse models)
613393 Birbeck Granule Deficiency
605808 Birdshot Chorioretinopathy (1 mouse models)
612292 Birk-Barel Mental Retardation Dysmorphism Syndrome
135150 Birt-Hogg-Dube Syndrome; BHD (2 mouse models)
222800 Bisphosphoglycerate Mutase Deficiency
262000 Bjornstad Syndrome; BJS
109800 Bladder Cancer (6 mouse models)
109820 Bladder Diverticulum
186580 Blau Syndrome
605913 Bleeding Disorder, East Texas Type
614201 Bleeding Disorder, Platelet-Type, 11; BDPLT11
605735 Bleeding Disorder, Platelet-Type, 12; BDPLT12
614009 Bleeding Disorder, Platelet-Type, 13, Susceptibility To; BDPLT13
614158 Bleeding Disorder, Platelet-Type, 14; BDPLT14
615193 Bleeding Disorder, Platelet-Type, 15; BDPLT15
187800 Bleeding Disorder, Platelet-Type, 16; BDPLT16 (2 mouse models)
187900 Bleeding Disorder, Platelet-Type, 17; BDPLT17
609821 Bleeding Disorder, Platelet-Type, 8; BDPLT8
614200 Bleeding Disorder, Platelet-Type, 9; BDPLT9
109900 Blepharochalasis and Double Lip
110000 Blepharochalasis, Superior
119580 Blepharocheilodontic Syndrome; BCDS
110050 Blepharonasofacial Malformation Syndrome
110100 Blepharophimosis, Ptosis, and Epicanthus Inversus; BPES (2 mouse models)
615057 Blepharophimosis-Ptosis-Intellectual Disability Syndrome; BPIDS (1 mouse models)
604314 Blepharophimosis with Facial and Genital Anomalies and Mental Retardation
210745 Blepharophimosis with Ptosis, Syndactyly, and Short Stature
110150 Blepharoptosis, Myopia, and Ectopia Lentis
606798 Blepharospasm, Benign Essential
210900 Bloom Syndrome; BLM (7 mouse models)
259200 Blount Disease, Adolescent
188700 Blount Disease, Infantile
303700 Blue Cone Monochromacy; BCM
211000 Blue Diaper Syndrome
603670 Blue Nevi, Familial Multiple
112200 Blue Rubber Bleb Nevus
300054 Body Length, Mouse, Human Homolog
605039 Bohring-Opitz Syndrome; BOPS
211120 Bone Dysplasia, Lethal, Holmgren Type
612394 Bone Fragility with Contractures, Arterial Rupture, and Deafness
112240 Bone Fragility with Craniosynostosis, Ocular Proptosis, Hydrocephalus, and Distinctive Facial Features
614675 Bone Marrow Failure Syndrome 1; BMFS1
615715 Bone Marrow Failure Syndrome 2; BMFS2
112270 Bone Pain, Periodic
112300 Book Syndrome
112310 Boomerang Dysplasia
301900 Borjeson-Forssman-Lehmann Syndrome; BFLS
300843 Bornholm Eye Disease; BED
211170 Borrone Dermatocardioskeletal Syndrome
607475 Bothnia Retinal Dystrophy (1 mouse models)
215470 Boucher-Neuhauser Syndrome; BNHS
211180 Bowen-Conradi Syndrome; BWCNS
211200 Bowen Syndrome of Multiple Malformations
211355 Bowing of Long Bones, Asymmetric and Symmetric
601357 Brachial Amelia, Cleft Lip, and Holoprosencephaly; ACLH
608585 Brachial Palsy, Familial Congenital
211380 Brachioskeletogenital Syndrome
112370 Brachmann-De Lange-Like Facial Changes with Microcephaly, Metatarsus Adductus, and Developmental Delay
601353 Brachycephaly, Deafness, Cataract, Microstomia, and Mental Retardation
610023 Brachydactyly, Coloboma, and Anterior Segment Dysgenesis
112440 Brachydactyly, Combined B and E Types
113450 Brachydactyly-Distal Symphalangism Syndrome
113310 Brachydactyly-Ectrodactyly with Fibular Aplasia or Hypoplasia
602561 Brachydactyly, Intraventricular Septal Defect, and Deafness
600430 Brachydactyly-Mental Retardation Syndrome; BDMR
301940 Brachydactyly, Mononen Type
113400 Brachydactyly-Nystagmus-Cerebellar Ataxia
112450 Brachydactyly, Preaxial, with Hallux Varus and Thumb Abduction
610713 Brachydactyly-Syndactyly Syndrome
607004 Brachydactyly, Type A1, B; BDA1B
112500 Brachydactyly, Type A1; BDA1 (2 mouse models)
615072 Brachydactyly, Type A1, C; BDA1C (1 mouse models)
613627 Brachydactyly, Type A1, with Short Stature, Scoliosis, Microcephaly, Ptosis, Hearing Loss, and Mental Retardation
112600 Brachydactyly, Type A2; BDA2 (1 mouse models)
211369 Brachydactyly, Type A2, with Microcephaly
112700 Brachydactyly, Type A3; BDA3
112800 Brachydactyly, Type A4; BDA4
112910 Brachydactyly, Type A6; BDA6
113000 Brachydactyly, Type B1; BDB1
611377 Brachydactyly, Type B2; BDB2
113100 Brachydactyly, Type C; BDC (1 mouse models)
113200 Brachydactyly, Type D; BDD
113300 Brachydactyly, Type E1; BDE1
613382 Brachydactyly, Type E2; BDE2
113301 Brachydactyly, Type E, with Atrial Septal Defect, Type II
113470 Brachymesomelia-Renal Syndrome
211370 Brachymetapody-Anodontia-Hypotrichosis-Albinoidism
113475 Brachymetatarsus IV
113477 Brachymorphism-Onychodysplasia-Dysphalangism Syndrome
271530 Brachyolmia Type 1, Hobaek Type
271630 Brachyolmia Type 1, Toledo Type
613678 Brachyolmia Type 2
113500 Brachyolmia Type 3
612847 Brachyolmia Type 4 with Mild Epiphyseal and Metaphyseal Changes (1 mouse models)
609945 Brachyphalangy, Polydactyly, and Tibial Aplasia/Hypoplasia
113480 Brachytelephalangy with Characteristic Facies and Kallmann Syndrome
607595 Brain Small Vessel Disease with Hemorrhage
614923 Branched-Chain Ketoacid Dehydrogenase Kinase Deficiency; BCKDKD
301950 Branchial Arch Syndrome, X-Linked
113600 Branchial Cleft Anomalies
113610 Branchial Myoclonus with Spastic Paraparesis and Cerebellar Ataxia
609166 Branchiogenic-Deafness Syndrome
113620 Branchiooculofacial Syndrome; BOFS
602588 Branchiootic Syndrome 1; BOS1
120502 Branchiootic Syndrome 2
608389 Branchiootic Syndrome 3; BOS3
113650 Branchiootorenal Syndrome 1; BOR1 (5 mouse models)
610896 Branchiootorenal Syndrome 2; BOR2
114480 Breast Cancer (61 mouse models)
600048 Breast Cancer, 11-22 Translocation-Associated; BRCATA
605365 Breast Cancer 3; BRCA3
604370 Breast-Ovarian Cancer, Familial, Susceptibility to, 1; BROVCA1 (3 mouse models)
612555 Breast-Ovarian Cancer, Familial, Susceptibility to, 2; BROVCA2
613399 Breast-Ovarian Cancer, Familial, Susceptibility to, 3; BROVCA3
614291 Breast-Ovarian Cancer, Familial, Susceptibility to, 4; BROVCA4
113700 Breasts and Nipples, Absence of
607578 Breath-Holding Spells
603828 Brittle Bone Disorder
229200 Brittle Cornea Syndrome 1; BCS1
614170 Brittle Cornea Syndrome 2; BCS2
602071 Broad Terminal Phalanges, Familial
601003 Brody Myopathy
211400 Bronchiectasis with or without Elevated Sweat Chloride 1; BESC1
613021 Bronchiectasis with or without Elevated Sweat Chloride 2; BESC2
613071 Bronchiectasis with or without Elevated Sweat Chloride 3; BESC3
211450 Bronchomalacia
605041 Brooke-Spiegler Syndrome; BRSS
300612 Brooks-Wisniewski-Brown Syndrome
211530 Brown-Vialetto-Van Laere Syndrome 1; BVVLS1
614707 Brown-Vialetto-Van Laere Syndrome 2; BVVLS2
259450 Bruck Syndrome 1; BRKS1
609220 Bruck Syndrome 2; BRKS2
601144 Brugada Syndrome 1; BRGDA1 (2 mouse models)
611777 Brugada Syndrome 2; BRGDA2
611875 Brugada Syndrome 3; BRGDA3
611876 Brugada Syndrome 4; BRGDA4
612838 Brugada Syndrome 5; BRGDA5
613119 Brugada Syndrome 6; BRGDA6
613120 Brugada Syndrome 7; BRGDA7 (1 mouse models)
613123 Brugada Syndrome 8; BRGDA8
300615 Brunner Syndrome (1 mouse models)
600880 Budd-Chiari Syndrome; BDCHS
211480 Buerger Disease
607499 Bulimia Nervosa, Susceptibility to, 1; BULN1
610269 Bulimia Nervosa, Susceptibility to, 2; BULN2
302000 Bullous Dystrophy, Hereditary Macular Type
113950 Bundle Branch Block, Familial Isolated Complete Right
113970 Burkitt Lymphoma; BL (5 mouse models)
608572 Burn-McKeown Syndrome
610446 Buruli Ulcer, Susceptibility to
166700 Buschke-Ollendorff Syndrome; BOS
177400 Butyrylcholinesterase; BCHE (1 mouse models)
113960 Butyrylesterase 1

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last database update
04/08/2014
MGI 5.17
The Jackson Laboratory