Prune belly syndrome
ORPHA:29703C syndrome
ORPHA:73M syndrome
ORPHA:2616Absence of fingerprints-congenital milia syndrome
ORPHA:1658Acquired partial lipodystrophy
ORPHA:79087Acropectorovertebral dysplasia
ORPHA:957Antisynthetase syndrome
ORPHA:81Ataxia-telangiectasia
ORPHA:100Autosomal recessive multiple pterygium syndrome
ORPHA:2990B-cell immunodeficiency-limb anomaly-urogenital malformation syndrome
ORPHA:567502Balint syndrome
ORPHA:363746Ballard syndrome
ORPHA:93395Bamforth-Lazarus syndrome
ORPHA:1226Bangstad syndrome
ORPHA:1227Banki syndrome
ORPHA:1228Barber-Say syndrome
ORPHA:1231Bardet-Biedl syndrome
ORPHA:110Barth syndrome
ORPHA:111Bartsocas-Papas syndrome
ORPHA:1234Bartter 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:1239Bencze syndrome
ORPHA:1241BIDS 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:1299BRESEK syndrome
ORPHA:85284Bruck syndrome
ORPHA:2771C syndrome
ORPHA:1308CANDLE syndrome
ORPHA:325004Cataract-nephropathy-encephalopathy syndrome
ORPHA:1380Celiac artery compression syndrome
ORPHA:293208CHAND syndrome
ORPHA:1401