Camptodactyly-arthropathy-coxa-vara-pericarditis syndrome
ORPHA:2848Cancer-associated retinopathy
ORPHA:71505Cardiac anomalies-short stature-joint hypermobility-facial dysmorphism syndrome
ORPHA:228410Cardiofaciocutaneous syndrome
ORPHA:1340Carnevale syndrome
ORPHA:2998Cataract-nephropathy-encephalopathy syndrome
ORPHA:1380Chronic intestinal pseudoobstruction syndrome
ORPHA:2978CK syndrome
ORPHA:251383Congenital cataract-hearing loss-severe developmental delay syndrome
ORPHA:300313Congenital 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:171839CREST syndrome
ORPHA:90290Curly hair-acral keratoderma-caries syndrome
ORPHA:307766Deafness 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:3411Drug reaction with eosinophilia and systemic symptoms
ORPHA:139402Ectrodactyly-cleft palate syndrome
ORPHA:1889EEC syndrome
ORPHA:1896EEM syndrome
ORPHA:1897Endocrine-cerebro-osteodysplasia syndrome
ORPHA:199332Erythrokeratodermia-cardiomyopathy syndrome
ORPHA:476096Feingold syndrome
ORPHA:1305Focal facial dermal dysplasia type I
ORPHA:79133Glossopalatine ankylosis
ORPHA:141163GMS syndrome
ORPHA:2090Gorlin-Chaudhry-Moss syndrome
ORPHA:2095H syndrome
ORPHA:168569HEC syndrome
ORPHA:2119Hemiconvulsion-hemiplegia-epilepsy syndrome
ORPHA:86908Hemidystonia-hemiatrophy syndrome
ORPHA:306741Hyperornithinemia-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:453