CK syndrome
ORPHA:251383COFS syndrome
ORPHA:1466Congenital contractural arachnodactyly
ORPHA:115Congenital generalized hypertrichosis, Ambras type
ORPHA:1023Congenital 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:85199Cutis verticis gyrata-thyroid aplasia-intellectual disability syndrome
ORPHA:79482Diencephalic syndrome
ORPHA:1672Diethylstilbestrol syndrome
ORPHA:1916Digitorenocerebral syndrome
ORPHA:1674Distal deletion 3p syndrome
ORPHA:1620Double uterus-hemivagina-renal agenesis syndrome
ORPHA:3411Ectrodactyly-cleft palate syndrome
ORPHA:1889EEC syndrome
ORPHA:1896EEM syndrome
ORPHA:1897Endocrine-cerebro-osteodysplasia syndrome
ORPHA:199332Erythrokeratodermia-cardiomyopathy syndrome
ORPHA:476096Familial caudal dysgenesis
ORPHA:1768GMS syndrome
ORPHA:2090Gorlin-Chaudhry-Moss syndrome
ORPHA:2095H syndrome
ORPHA:168569HEC syndrome
ORPHA:2119Helsmoortel-Van der Aa syndrome
ORPHA:404448Hemiconvulsion-hemiplegia-epilepsy syndrome
ORPHA:86908Hereditary leiomyomatosis and renal cell cancer
ORPHA:523HNF1B-related autosomal dominant tubulointerstitial kidney disease
ORPHA:93111Holmes-Adie syndrome
ORPHA:454718Hydrocephalus-costovertebral dysplasia-Sprengel anomaly syndrome
ORPHA:2180Hyperornithinemia-hyperammonemia-homocitrullinuria syndrome
ORPHA:415Hypertelorism-microtia-facial clefting syndrome
ORPHA:2213Hypohidrotic ectodermal dysplasia-hypothyroidism-ciliary dyskinesia syndrome
ORPHA:1882Hypomyelination-hypogonadotropic hypogonadism-hypodontia syndrome
ORPHA:88637Hypoparathyroidism-sensorineural deafness-renal disease syndrome
ORPHA:2237IBIDS syndrome
ORPHA:453ICF syndrome
ORPHA:2268Iridocorneal endothelial syndrome
ORPHA:64734JMP syndrome
ORPHA:324999Joubert syndrome with oculorenal defect
ORPHA:2318KBG syndrome
ORPHA:2332KID syndrome
ORPHA:477L1 syndrome
ORPHA:275543Laryngo-onycho-cutaneous syndrome
ORPHA:2407Lethal ataxia with deafness and optic atrophy
ORPHA:1187Mammary-digital-nail syndrome
ORPHA:238744Mandibular hypoplasia-deafness-progeroid features-lipodystrophy syndrome
ORPHA:363649