Cardiac anomalies-short stature-joint hypermobility-facial dysmorphism syndrome
ORPHA:228410Cardiofaciocutaneous syndrome
ORPHA:1340Cardiospondylocarpofacial syndrome
ORPHA:3238Carnevale syndrome
ORPHA:2998Carney complex
ORPHA:1359Cataract-nephropathy-encephalopathy syndrome
ORPHA:1380Choroidal atrophy-alopecia syndrome
ORPHA:1433Chronic intestinal pseudoobstruction syndrome
ORPHA:2978CK syndrome
ORPHA:251383CNTNAP2-related developmental and epileptic encephalopathy
ORPHA:163681Congenital contractural arachnodactyly
ORPHA:115Congenital muscular dystrophy-infantile cataract-hypogonadism syndrome
ORPHA:1875Congenital 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:85199Craniosynostosis-hydrocephalus-Arnold-Chiari malformation type I-radioulnar synostosis syndrome
ORPHA:171839Deafness with labyrinthine aplasia, microtia, and microdontia
ORPHA:90024Dent disease
ORPHA:1652Diethylstilbestrol syndrome
ORPHA:1916Digitorenocerebral syndrome
ORPHA:1674Distal deletion 3p syndrome
ORPHA:1620Donnai-Barrow syndrome
ORPHA:2143DOORS syndrome
ORPHA:79500Double uterus-hemivagina-renal agenesis syndrome
ORPHA:3411Down syndrome
ORPHA:870EAST syndrome
ORPHA:199343Ectrodactyly-cleft palate syndrome
ORPHA:1889EEC syndrome
ORPHA:1896EEM syndrome
ORPHA:1897Endocrine-cerebro-osteodysplasia syndrome
ORPHA:199332Erythrokeratodermia-cardiomyopathy syndrome
ORPHA:476096Familial dysautonomia
ORPHA:1764Feingold syndrome
ORPHA:1305Focal facial dermal dysplasia type I
ORPHA:79133Fragile X syndrome
ORPHA:908Frey syndrome
ORPHA:662240GMS syndrome
ORPHA:2090Gorlin-Chaudhry-Moss syndrome
ORPHA:2095H syndrome
ORPHA:168569Hajdu-Cheney syndrome
ORPHA:955HEC syndrome
ORPHA:2119Hemiconvulsion-hemiplegia-epilepsy syndrome
ORPHA:86908Hemidystonia-hemiatrophy syndrome
ORPHA:306741Holmes-Adie syndrome
ORPHA:454718Hyperornithinemia-hyperammonemia-homocitrullinuria syndrome
ORPHA:415Hypertelorism-microtia-facial clefting syndrome
ORPHA:2213