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List of all diseases starting with B

• BARTH SYNDROME (BTHS) MIM=302060
• BARTTER SYNDROME, TYPE 1, ANTENATAL; BARTS1 MIM=601678
• BARTTER SYNDROME, TYPE 2, ANTENATAL; BARTS2 MIM=241200
• BARTTER SYNDROME, TYPE 3; BARTS3 MIM=607364
• BARTTER SYNDROME, TYPE 4A, NEONATAL, WITH SENSORINEURAL DEAFNESS; BARTS4A MIM=602522
• BARTTER SYNDROME, TYPE 4B, NEONATAL, WITH SENSORINEURAL DEAFNESS; BARTS4B MIM=613090
• BARTTER SYNDROME, TYPE 5, ANTENATAL, TRANSIENT (BARTS5) MIM=300971
• BARTTER-LIKE-SYNDROME [DD] MIM=---
• BECKWITH-WIEDEMANN SYNDROME. EXOMPHALOS-MAKROGLOSSIA-GIGANTISM SYNDROME (BWS) MIM=130650
• BEHR SYNDROME (BEHRS) MIM=210000
• BENIGN INFANTILE MITOCHONDRIAL MYOPATHY (BIMM) MIM=500009
• BENIGN INFANTILE MITOCHONDRIAL MYOPATHY AND CARDIOMYOPATHY (BIMC) MIM=
• BETA-AMINOISOBUTYRIC ACIDURIA (BAIBA) MIM=210100
• BETA-KETOTHIOLASE DEFICIENCY; ALPHA-METHYLACETOACETIC ACIDURIA MIM=203750
• BETA-MANNOSIDOSIS MIM=248510
• BETA-MERCAPTOLACTATE-CYSTEINE DISULFIDURIA MIM=249650
• BILE ACID SYNTHESIS DEFECT, CONGENITAL, 1 (CBAS1) MIM=607765
• BILE ACID SYNTHESIS DEFECT, CONGENITAL, 2 (CBAS2) MIM=235555
• BILE ACID SYNTHESIS DEFECT, CONGENITAL, 3 (CBAS3) MIM=613812
• BILE ACID SYNTHESIS DEFECT, CONGENITAL, 4 (CBAS4) MIM=214950
• BILE ACID SYNTHESIS DEFECT, CONGENITAL, 5 (CBAS5) MIM=616278
• BILE ACID SYNTHESIS DEFECT, CONGENITAL, 6; CBAS6 MIM=617308
• BIOTINIDASE DEFICIENCY MIM=253260
• BLUE DIAPER SYNDROME MIM=211000
• BRANCHED-CHAIN AMINOTRANSFERASE 2 (BCAT2) MIM=113530
• BRANCHED-CHAIN KETO ACID DEHYDROGENASE KINASE DEFICIENCY (BCKDKD) MIM=614923
• BROWN-VIALETTO-VAN LAERE SYNDROME 1 (BVVLS1) MIM=211530
• BROWN-VIALETTO-VAN LAERE SYNDROME 2 (BVVLS2) MIM=614707
• BRUNNER SYNDROME (MONOAMINE OXIDASE-A DEFICIENCY (MAO-A) MIM=300615
• BUTYROBETAINE-GAMMA,2-OXOGLUTARATE DIOXYGENASE 1; BBOX1 MIM=603312