Curly hair-acral keratoderma-caries syndrome
ORPHA:307766Deafness with labyrinthine aplasia, microtia, and microdontia
ORPHA:90024Diethylstilbestrol syndrome
ORPHA:1916Digitorenocerebral syndrome
ORPHA:1674Distal deletion 3p syndrome
ORPHA:1620Double uterus-hemivagina-renal agenesis syndrome
ORPHA:3411Down syndrome
ORPHA:870EAST syndrome
ORPHA:199343Ectrodactyly-cleft palate syndrome
ORPHA:1889EDICT syndrome
ORPHA:293936EEC syndrome
ORPHA:1896EEM syndrome
ORPHA:1897Ehlers-Danlos/osteogenesis imperfecta syndrome
ORPHA:230857Eiken syndrome
ORPHA:79106Emanuel syndrome
ORPHA:96170EN1-related dorsoventral syndrome
ORPHA:611223Endocrine-cerebro-osteodysplasia syndrome
ORPHA:199332Eng-Strom syndrome
ORPHA:1937Epstein syndrome
ORPHA:1019Erythrokeratodermia-cardiomyopathy syndrome
ORPHA:476096Evans syndrome
ORPHA:1959Facial dysmorphism-immunodeficiency-livedo-short stature syndrome
ORPHA:352712Febrile infection-related epilepsy syndrome
ORPHA:163703Feingold syndrome
ORPHA:1305Frey syndrome
ORPHA:662240GAPO syndrome
ORPHA:2067GMS syndrome
ORPHA:2090Gorlin-Chaudhry-Moss syndrome
ORPHA:2095GRACILE syndrome
ORPHA:53693H syndrome
ORPHA:168569HARP syndrome
ORPHA:157855HEC syndrome
ORPHA:2119Hemiconvulsion-hemiplegia-epilepsy syndrome
ORPHA:86908Hemidystonia-hemiatrophy syndrome
ORPHA:306741HNF1B-related autosomal dominant tubulointerstitial kidney disease
ORPHA:93111Holmes-Adie syndrome
ORPHA:454718Hyperinsulinism-hyperammonemia syndrome
ORPHA:35878Hyperornithinemia-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:2237Hypotrichosis-osteolysis-periodontitis-palmoplantar keratoderma syndrome
ORPHA:307936IBIDS syndrome
ORPHA:453ICF syndrome
ORPHA:2268Iridocorneal endothelial syndrome
ORPHA:64734JMP syndrome
ORPHA:324999Joubert syndrome with hepatic defect
ORPHA:1454