Global developmental delay-alopecia-macrocephaly-facial dysmorphism-structural brain anomalies syndrome
ORPHA:5444883C syndrome
ORPHA:73M syndrome
ORPHA:2616Absence of fingerprints-congenital milia syndrome
ORPHA:1658Acropectorovertebral dysplasia
ORPHA:957Antisynthetase syndrome
ORPHA:81Ataxia-telangiectasia
ORPHA:100Autoimmune polyendocrinopathy type 2
ORPHA:3143Autosomal dominant hyper-IgE syndrome due to STAT3 deficiency
ORPHA:2314Autosomal dominant intellectual disability-craniofacial dysmorphism-macrocephaly-hypotonia syndrome due to H1-4 mutation
ORPHA:642763B-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:1231Barth syndrome
ORPHA:111Bartter syndrome
ORPHA:112Bazex syndrome
ORPHA:166113Beckwith-Wiedemann syndrome
ORPHA:116Behr 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:1308CACH syndrome
ORPHA:135Cataract-nephropathy-encephalopathy syndrome
ORPHA:1380CHAND syndrome
ORPHA:1401CK syndrome
ORPHA:251383Congenital contractural arachnodactyly
ORPHA:115Congenital muscular dystrophy-infantile cataract-hypogonadism syndrome
ORPHA:1875Cornelia de Lange syndrome
ORPHA:199Corpus callosum agenesis-neuronopathy syndrome
ORPHA:1496