Infantile hypotonia-oculomotor anomalies-hyperkinetic movements-developmental delay syndrome
ORPHA:5220773C syndrome
ORPHA:73M syndrome
ORPHA:261646,XY complete gonadal dysgenesis
ORPHA:242Absence of fingerprints-congenital milia syndrome
ORPHA:1658Acrogeria
ORPHA:2500Acropectorovertebral dysplasia
ORPHA:957Aniridia-intellectual disability syndrome
ORPHA:1068Antisynthetase syndrome
ORPHA:81Ascher syndrome
ORPHA:1253Ataxia-deafness-intellectual disability syndrome
ORPHA:1188Ataxia-telangiectasia
ORPHA:100Autosomal dominant spastic paraplegia type 17
ORPHA:100998Autosomal recessive spastic paraplegia type 20
ORPHA:101000Autosomal recessive spastic paraplegia type 23
ORPHA:101003Axenfeld-Rieger syndrome
ORPHA:782B-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:1228Barber-Say syndrome
ORPHA:1231Barth 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:166113Becker nevus syndrome
ORPHA:64755Behr 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:1299