Segmental venous malformation
ORPHA:2170083C syndrome
ORPHA:73M syndrome
ORPHA:261646,XY complete gonadal dysgenesis
ORPHA:242Absence of fingerprints-congenital milia syndrome
ORPHA:1658Acropectorovertebral dysplasia
ORPHA:957Antisynthetase syndrome
ORPHA:81Ascher syndrome
ORPHA:1253Autosomal dominant spastic paraplegia type 17
ORPHA:100998Autosomal recessive spastic paraplegia type 20
ORPHA:101000Axenfeld-Rieger syndrome
ORPHA:782B-cell immunodeficiency-limb anomaly-urogenital malformation syndrome
ORPHA:567502Balint syndrome
ORPHA:363746Banki syndrome
ORPHA:1228Barber-Say syndrome
ORPHA:1231Barth syndrome
ORPHA:111Bartter syndrome
ORPHA:112Bazex syndrome
ORPHA:166113Becker nevus syndrome
ORPHA:64755Behr syndrome
ORPHA:1239Bencze syndrome
ORPHA:1241BIDS syndrome
ORPHA:1245Biliary atresia with splenic malformation syndrome
ORPHA:244283Blau 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:1292Braddock syndrome
ORPHA:52047Branchioskeletogenital syndrome
ORPHA:1299BRESEK syndrome
ORPHA:85284Bruck syndrome
ORPHA:2771C syndrome
ORPHA:1308Cataract-nephropathy-encephalopathy syndrome
ORPHA:1380Childhood disintegrative disorder
ORPHA:168782CHIME syndrome
ORPHA:3474CK syndrome
ORPHA:251383Congenital contractural arachnodactyly
ORPHA:115Congenital muscular dystrophy-infantile cataract-hypogonadism syndrome
ORPHA:1875CPE-related Prader-Willi-like syndrome
ORPHA:633028Craniosynostosis-hydrocephalus-Arnold-Chiari malformation type I-radioulnar synostosis syndrome
ORPHA:171839Deafness-enamel hypoplasia-nail defects syndrome
ORPHA:3220Distal deletion 3p syndrome
ORPHA:1620