Down syndrome
ORPHA:870Early-onset parkinsonism-intellectual disability syndrome
ORPHA:2379EAST syndrome
ORPHA:199343Ectrodactyly-cleft palate syndrome
ORPHA:1889EEC syndrome
ORPHA:1896EEM syndrome
ORPHA:1897Endocrine-cerebro-osteodysplasia syndrome
ORPHA:199332Endosteal hyperostosis, Worth type
ORPHA:2790Erythrokeratodermia-cardiomyopathy syndrome
ORPHA:476096Facial dysmorphism-immunodeficiency-livedo-short stature syndrome
ORPHA:352712Febrile infection-related epilepsy syndrome
ORPHA:163703Feingold syndrome
ORPHA:1305Fragile X syndrome
ORPHA:908Frey syndrome
ORPHA:662240GAPO syndrome
ORPHA:2067Gingival fibromatosis-aortic root dilatation-facial dysmorphism-intellectual disability syndrome
ORPHA:664438GMS syndrome
ORPHA:2090Gorlin-Chaudhry-Moss syndrome
ORPHA:2095H syndrome
ORPHA:168569HARP syndrome
ORPHA:157855HEC syndrome
ORPHA:2119Hemiconvulsion-hemiplegia-epilepsy syndrome
ORPHA:86908Hemidystonia-hemiatrophy syndrome
ORPHA:306741Hereditary acrokeratotic poikiloderma
ORPHA:2907Holmes-Adie syndrome
ORPHA:454718Hyperinsulinism-hyperammonemia syndrome
ORPHA:35878Hyperornithinemia-hyperammonemia-homocitrullinuria syndrome
ORPHA:415Hypertelorism-microtia-facial clefting syndrome
ORPHA:2213Hypodontia-dysplasia of nails syndrome
ORPHA:2228Hypohidrotic ectodermal dysplasia-hypothyroidism-ciliary dyskinesia syndrome
ORPHA:1882Hypomyelination-hypogonadotropic hypogonadism-hypodontia syndrome
ORPHA:88637Hypoparathyroidism-sensorineural deafness-renal disease syndrome
ORPHA:2237IBIDS syndrome
ORPHA:453ICF syndrome
ORPHA:2268Ichthyosis follicularis-alopecia-photophobia syndrome
ORPHA:2273Iridocorneal endothelial syndrome
ORPHA:64734JMP syndrome
ORPHA:324999KBG syndrome
ORPHA:2332Kenny-Caffey syndrome
ORPHA:2333KID syndrome
ORPHA:477L1 syndrome
ORPHA:275543Laryngo-onycho-cutaneous syndrome
ORPHA:2407Lethal ataxia with deafness and optic atrophy
ORPHA:1187Lethal hemolytic anemia-genital anomalies syndrome
ORPHA:1046LIG4 syndrome
ORPHA:99812Limb body wall complex
ORPHA:2369Mammary-digital-nail syndrome
ORPHA:238744Mandibular hypoplasia-deafness-progeroid features-lipodystrophy syndrome
ORPHA:363649