Maxillonasal dysplasia
ORPHA:124821q deletion syndrome
ORPHA:5743C syndrome
ORPHA:73M syndrome
ORPHA:26163MC syndrome
ORPHA:29384346,XY complete gonadal dysgenesis
ORPHA:24247,XYY syndrome
ORPHA:8Absence of fingerprints-congenital milia syndrome
ORPHA:1658Acropectorovertebral dysplasia
ORPHA:957Alport syndrome-intellectual disability-midface hypoplasia-elliptocytosis syndrome
ORPHA:86818Andersen-Tawil syndrome
ORPHA:37553ANE syndrome
ORPHA:157954Angora hair nevus
ORPHA:370039Ankyloblepharon-ectodermal defects-cleft lip/palate syndrome
ORPHA:1071Antisynthetase syndrome
ORPHA:81Antley-Bixler syndrome
ORPHA:83Arthrogryposis-renal dysfunction-cholestasis syndrome
ORPHA:2697Ascher syndrome
ORPHA:1253Autoimmune polyendocrinopathy type 1
ORPHA:3453Autosomal dominant hyper-IgE syndrome due to STAT3 deficiency
ORPHA:2314Autosomal 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:363746Ballard syndrome
ORPHA:93395Banki syndrome
ORPHA:1228Barber-Say syndrome
ORPHA:1231Barth syndrome
ORPHA:111Bartter syndrome
ORPHA:112Bazex 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:1271Brachydactyly-nystagmus-cerebellar ataxia syndrome
ORPHA:1246Brachymorphism-onychodysplasia-dysphalangism syndrome
ORPHA:1292Branchioskeletogenital syndrome
ORPHA:1299