Cardiofaciocutaneous syndrome
ORPHA:1340Carnevale syndrome
ORPHA:2998Cataract-nephropathy-encephalopathy syndrome
ORPHA:1380Childhood disintegrative disorder
ORPHA:168782Chronic intestinal pseudoobstruction syndrome
ORPHA:2978CK syndrome
ORPHA:251383CNTNAP2-related developmental and epileptic encephalopathy
ORPHA:163681Congenital contractural arachnodactyly
ORPHA:115Congenital generalized lipodystrophy
ORPHA:528Congenital 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:171839Dent disease
ORPHA:1652Diencephalic syndrome
ORPHA:1672Diethylstilbestrol 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:199332Epidermolysis bullosa simplex with anodontia/hypodontia
ORPHA:2325Erythrokeratodermia-cardiomyopathy syndrome
ORPHA:476096Feingold syndrome
ORPHA:1305Focal facial dermal dysplasia type I
ORPHA:79133Fragile X syndrome
ORPHA:908GMS syndrome
ORPHA:2090Gorlin syndrome
ORPHA:377Gorlin-Chaudhry-Moss syndrome
ORPHA:2095Griscelli syndrome
ORPHA:381H syndrome
ORPHA:168569HARP syndrome
ORPHA:157855Hearing loss-familial salivary gland insensitivity to aldosterone syndrome
ORPHA:3225HEC syndrome
ORPHA:2119HELLP syndrome
ORPHA:244242Hemiconvulsion-hemiplegia-epilepsy syndrome
ORPHA:86908Hemidystonia-hemiatrophy syndrome
ORPHA:306741Holmes-Adie syndrome
ORPHA:454718Hyperornithinemia-hyperammonemia-homocitrullinuria syndrome
ORPHA:415