Orofaciodigital syndrome type 4
ORPHA:275346,XY complete gonadal dysgenesis
ORPHA:242Absence of fingerprints-congenital milia syndrome
ORPHA:1658Acquired partial lipodystrophy
ORPHA:79087Acropectorovertebral dysplasia
ORPHA:957Ataxia-deafness-intellectual disability syndrome
ORPHA:1188Ataxia-telangiectasia
ORPHA:100Autosomal dominant hyper-IgE syndrome due to STAT3 deficiency
ORPHA:2314Autosomal dominant spastic paraplegia type 17
ORPHA:100998B-cell immunodeficiency-limb anomaly-urogenital malformation syndrome
ORPHA:567502Balint syndrome
ORPHA:363746Ballard syndrome
ORPHA:93395Baller-Gerold syndrome
ORPHA:1225Bamforth-Lazarus syndrome
ORPHA:1226Bangstad syndrome
ORPHA:1227Banki syndrome
ORPHA:1228Baraitser-Winter cerebrofrontofacial syndrome
ORPHA:2995Barber-Say syndrome
ORPHA:1231Bardet-Biedl syndrome
ORPHA:110Barth syndrome
ORPHA:111Bartter syndrome
ORPHA:112Bartter syndrome type 1
ORPHA:620217Bartter syndrome type 2
ORPHA:620220Bartter syndrome type 3
ORPHA:93605Bartter syndrome type 4
ORPHA:89938Bazex syndrome
ORPHA:166113Behr syndrome
ORPHA:1239BIDS syndrome
ORPHA:1245Biliary atresia with splenic malformation syndrome
ORPHA:244283Birk-Barel syndrome
ORPHA:166108Blau syndrome
ORPHA:90340Blepharo-cheilo-odontic syndrome
ORPHA:1997Bloom syndrome
ORPHA:125Blue rubber bleb nevus
ORPHA:1059BNAR syndrome
ORPHA:217266Bohring-Opitz syndrome
ORPHA:97297Böök syndrome
ORPHA:1262BOR syndrome
ORPHA:107Bowen syndrome
ORPHA:1271Brachymorphism-onychodysplasia-dysphalangism syndrome
ORPHA:1292Branchioskeletogenital syndrome
ORPHA:1299Bruck syndrome
ORPHA:2771Burn-McKeown syndrome
ORPHA:1200Burning mouth syndrome
ORPHA:353253C syndrome
ORPHA:1308Cataract-deafness-hypogonadism syndrome
ORPHA:1383CHAND syndrome
ORPHA:1401Clark-Baraitser syndrome
ORPHA:600731