Cardiac anomalies-short stature-joint hypermobility-facial dysmorphism syndrome
ORPHA:228410Cardiofaciocutaneous syndrome
ORPHA:1340Carnevale syndrome
ORPHA:2998Cataract-nephropathy-encephalopathy syndrome
ORPHA:1380Celiac artery compression syndrome
ORPHA:293208Chronic intestinal pseudoobstruction syndrome
ORPHA:2978CK syndrome
ORPHA:251383Complement hyperactivation-angiopathic thrombosis-protein-losing enteropathy syndrome
ORPHA:566175Congenital contractural arachnodactyly
ORPHA:115Congenital generalized hypertrichosis, Ambras type
ORPHA:1023Congenital sideroblastic anemia-B-cell immunodeficiency-periodic fever-developmental delay syndrome
ORPHA:369861Constitutional mismatch repair deficiency syndrome
ORPHA:252202Contractures-webbed neck-micrognathia-hypoplastic nipples syndrome
ORPHA:314002Corneodermatoosseous syndrome
ORPHA:3194Costello syndrome
ORPHA:3071CPE-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:90024Deficiency in anterior pituitary function-variable immunodeficiency syndrome
ORPHA:293978DEND syndrome
ORPHA:79134Dent disease
ORPHA:1652Denys-Drash syndrome
ORPHA:220Diethylstilbestrol syndrome
ORPHA:1916Digitorenocerebral syndrome
ORPHA:1674Dilated cardiomyopathy with ataxia
ORPHA:66634Distal deletion 3p syndrome
ORPHA:1620Dobrow syndrome
ORPHA:3262Donohue syndrome
ORPHA:508DOORS syndrome
ORPHA:79500Double uterus-hemivagina-renal agenesis syndrome
ORPHA:3411Down syndrome
ORPHA:870Dravet syndrome
ORPHA:33069Drug reaction with eosinophilia and systemic symptoms
ORPHA:139402Duane retraction syndrome
ORPHA:233Dursun syndrome
ORPHA:178503DYRK1A-related intellectual disability syndrome
ORPHA:464306Ectrodactyly-cleft palate syndrome
ORPHA:1889EEC syndrome
ORPHA:1896EEM syndrome
ORPHA:1897Endocrine-cerebro-osteodysplasia syndrome
ORPHA:199332Epilepsy with myoclonic-atonic seizures
ORPHA:1942Ermine phenotype
ORPHA:999Erythrokeratodermia-cardiomyopathy syndrome
ORPHA:476096Febrile infection-related epilepsy syndrome
ORPHA:163703Fibular aplasia-complex brachydactyly syndrome
ORPHA:2639Frey syndrome
ORPHA:662240