Cancer-associated retinopathy
ORPHA:71505CANDLE syndrome
ORPHA:325004CANOMAD syndrome
ORPHA:71279Cardiac anomalies-short stature-joint hypermobility-facial dysmorphism syndrome
ORPHA:228410Cardiofaciocutaneous syndrome
ORPHA:1340Carnevale syndrome
ORPHA:2998Cataract-nephropathy-encephalopathy syndrome
ORPHA:1380CHAND syndrome
ORPHA:1401Chronic intestinal pseudoobstruction syndrome
ORPHA:2978CK syndrome
ORPHA:251383Cohen syndrome
ORPHA:193Congenital cataract-hypertrophic cardiomyopathy-mitochondrial myopathy syndrome
ORPHA:1369Congenital contractural arachnodactyly
ORPHA:115Congenital generalized hypertrichosis, Ambras type
ORPHA:1023Congenital sideroblastic anemia-B-cell immunodeficiency-periodic fever-developmental delay syndrome
ORPHA:369861Corneodermatoosseous syndrome
ORPHA:3194Corpus callosum agenesis-neuronopathy syndrome
ORPHA:1496Costello syndrome
ORPHA:3071Cowden syndrome
ORPHA:201CPE-related Prader-Willi-like syndrome
ORPHA:633028Craniosynostosis-anal anomalies-porokeratosis syndrome
ORPHA:85199Curly hair-acral keratoderma-caries syndrome
ORPHA:307766Cutis verticis gyrata-thyroid aplasia-intellectual disability syndrome
ORPHA:79482Deafness with labyrinthine aplasia, microtia, and microdontia
ORPHA:90024Deafness-opticoacoustic nerve atrophy-dementia syndrome
ORPHA:3213Dent disease
ORPHA:1652Diethylstilbestrol 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:1897Eiken syndrome
ORPHA:79106Endocrine-cerebro-osteodysplasia syndrome
ORPHA:199332Erythrokeratodermia-cardiomyopathy syndrome
ORPHA:476096Feingold syndrome
ORPHA:1305Fragile X syndrome
ORPHA:908Frey syndrome
ORPHA:662240GMS syndrome
ORPHA:2090Gorlin-Chaudhry-Moss syndrome
ORPHA:2095H syndrome
ORPHA:168569HEC syndrome
ORPHA:2119Helsmoortel-Van der Aa syndrome
ORPHA:404448Hemiconvulsion-hemiplegia-epilepsy syndrome
ORPHA:86908Holmes-Adie syndrome
ORPHA:454718Hyperornithinemia-hyperammonemia-homocitrullinuria syndrome
ORPHA:415Hypertelorism-microtia-facial clefting syndrome
ORPHA:2213