Laron syndrome with immunodeficiency
ORPHA:22046521q deletion syndrome
ORPHA:5743C syndrome
ORPHA:73M syndrome
ORPHA:26163MC syndrome
ORPHA:29384347,XYY syndrome
ORPHA:8Abruzzo-Erickson syndrome
ORPHA:921Acquired generalized lipodystrophy
ORPHA:79086Acrocardiofacial syndrome
ORPHA:2008Acrogeria
ORPHA:2500Acropectorovertebral 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:81Aplastic anemia-intellectual disability-dwarfism syndrome
ORPHA:611216Arthrogryposis-renal dysfunction-cholestasis syndrome
ORPHA:2697Autoimmune polyendocrinopathy type 1
ORPHA:3453Autosomal dominant hyper-IgE syndrome due to STAT3 deficiency
ORPHA:2314Autosomal recessive faciodigitogenital syndrome
ORPHA:1974Autosomal recessive spastic paraplegia type 23
ORPHA:101003Ballard syndrome
ORPHA:93395Blepharo-cheilo-odontic syndrome
ORPHA:1997Body skin hyperlaxity due to vitamin K-dependent coagulation factor deficiency
ORPHA:91135Bohring-Opitz syndrome
ORPHA:97297BOR syndrome
ORPHA:107Brachydactyly-elbow wrist dysplasia syndrome
ORPHA:1275Brachymorphism-onychodysplasia-dysphalangism syndrome
ORPHA:1292Branchioskeletogenital syndrome
ORPHA:1299C syndrome
ORPHA:1308Cancer-associated retinopathy
ORPHA:71505Cardiac anomalies-short stature-joint hypermobility-facial dysmorphism syndrome
ORPHA:228410Cardiofaciocutaneous syndrome
ORPHA:1340Carnevale syndrome
ORPHA:2998Caroli syndrome
ORPHA:480520Cataract-nephropathy-encephalopathy syndrome
ORPHA:1380Christianson syndrome
ORPHA:85278Chronic intestinal pseudoobstruction syndrome
ORPHA:2978CK syndrome
ORPHA:251383Congenital brachyesophagus-intrathoracic stomach-vertebral anomalies syndrome
ORPHA:514352Congenital contractural arachnodactyly
ORPHA:115Congenital sideroblastic anemia-B-cell immunodeficiency-periodic fever-developmental delay syndrome
ORPHA:369861Corneodermatoosseous syndrome
ORPHA:3194Costello syndrome
ORPHA:3071CPE-related Prader-Willi-like syndrome
ORPHA:633028Craniosynostosis-anal anomalies-porokeratosis syndrome
ORPHA:85199Crouzon syndrome
ORPHA:207Cutis verticis gyrata-thyroid aplasia-intellectual disability syndrome
ORPHA:79482