Fragile X syndrome
ORPHA:9083C syndrome
ORPHA:73M syndrome
ORPHA:261646,XX testicular difference of sex development
ORPHA:39347,XYY syndrome
ORPHA:8Absence of fingerprints-congenital milia syndrome
ORPHA:1658Acropectorovertebral dysplasia
ORPHA:957Androgen insensitivity syndrome
ORPHA:754Angioosteohypotrophic syndrome
ORPHA:75508Anterior maxillary protrusion-strabismus-intellectual disability syndrome
ORPHA:562559Antisynthetase syndrome
ORPHA:81Autoimmune polyendocrinopathy type 1
ORPHA:3453Autosomal dominant hyper-IgE syndrome due to STAT3 deficiency
ORPHA:2314Autosomal recessive spastic paraplegia type 21
ORPHA:101001B-cell immunodeficiency-limb anomaly-urogenital malformation syndrome
ORPHA:567502Balint syndrome
ORPHA:363746Banki syndrome
ORPHA:1228Barth syndrome
ORPHA:111Bartter syndrome
ORPHA:112Bazex syndrome
ORPHA:166113Behr syndrome
ORPHA:1239Bencze syndrome
ORPHA:1241BIDS syndrome
ORPHA:1245Biliary atresia with splenic malformation syndrome
ORPHA:244283Blau syndrome
ORPHA:90340Blepharo-cheilo-odontic syndrome
ORPHA:1997Blepharospasm-oromandibular dystonia syndrome
ORPHA:93964Bloom 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:1308Cardiac anomalies-short stature-joint hypermobility-facial dysmorphism syndrome
ORPHA:228410Cardiofaciocutaneous syndrome
ORPHA:1340Carnevale syndrome
ORPHA:2998Cataract-intellectual disability-hypogonadism syndrome
ORPHA:1387Cataract-nephropathy-encephalopathy syndrome
ORPHA:1380Cerebral autosomal recessive arteriopathy-subcortical infarcts-leukoencephalopathy
ORPHA:199354Childhood disintegrative disorder
ORPHA:168782CK syndrome
ORPHA:251383Colobomatous macrophthalmia-microcornea syndrome
ORPHA:468672