Corneodermatoosseous syndrome
ORPHA:3194Costello syndrome
ORPHA:3071CPE-related Prader-Willi-like syndrome
ORPHA:633028Craniosynostosis-anal anomalies-porokeratosis syndrome
ORPHA:85199Craniosynostosis-intracranial calcifications syndrome
ORPHA:52054Deafness 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:464306Early-onset parkinsonism-intellectual disability syndrome
ORPHA:2379Ectrodactyly-cleft palate syndrome
ORPHA:1889EEC syndrome
ORPHA:1896EEM syndrome
ORPHA:1897Endocrine-cerebro-osteodysplasia syndrome
ORPHA:199332Eosinophilic fasciitis
ORPHA:3165Epilepsy with myoclonic-atonic seizures
ORPHA:1942Erythrokeratodermia-cardiomyopathy syndrome
ORPHA:476096Extrasystoles-short stature-hyperpigmentation-microcephaly syndrome
ORPHA:1964Familial partial lipodystrophy, Dunnigan type
ORPHA:2348Febrile infection-related epilepsy syndrome
ORPHA:163703Fibrous dysplasia/McCune-Albright syndrome
ORPHA:595216Fibular aplasia-complex brachydactyly syndrome
ORPHA:2639Fragile X-associated tremor/ataxia syndrome
ORPHA:93256Frey syndrome
ORPHA:662240German syndrome
ORPHA:2077GMS syndrome
ORPHA:2090Goodman syndrome
ORPHA:65798Gorlin-Chaudhry-Moss syndrome
ORPHA:2095Growth deficiency-brachydactyly-dysmorphism syndrome
ORPHA:2055H syndrome
ORPHA:168569HEC syndrome
ORPHA:2119Hemiconvulsion-hemiplegia-epilepsy syndrome
ORPHA:86908Hinman syndrome
ORPHA:84085