Vascular Ehlers-Danlos syndrome
ORPHA:28621q deletion syndrome
ORPHA:5743C syndrome
ORPHA:73M syndrome
ORPHA:26163MC syndrome
ORPHA:29384347,XYY syndrome
ORPHA:8Absence of fingerprints-congenital milia syndrome
ORPHA:1658Acquired partial lipodystrophy
ORPHA:79087Acropectorovertebral dysplasia
ORPHA:957Alport syndrome-intellectual disability-midface hypoplasia-elliptocytosis syndrome
ORPHA:86818ANE syndrome
ORPHA:157954Ankyloblepharon-ectodermal defects-cleft lip/palate syndrome
ORPHA:1071Antisynthetase syndrome
ORPHA:81Apparent mineralocorticoid excess
ORPHA:320Arthrogryposis-renal dysfunction-cholestasis syndrome
ORPHA:2697Ataxia-deafness-intellectual disability syndrome
ORPHA:1188Ataxia-telangiectasia
ORPHA:100Autoimmune polyendocrinopathy type 1
ORPHA:3453Autosomal dominant hyper-IgE syndrome due to STAT3 deficiency
ORPHA:2314Autosomal recessive multiple pterygium syndrome
ORPHA:2990B-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:1231Bardet-Biedl syndrome
ORPHA:110Barth syndrome
ORPHA:111Bartsocas-Papas syndrome
ORPHA:1234Bartter 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: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:1262