DOORS syndrome
ORPHA:79500Double uterus-hemivagina-renal agenesis syndrome
ORPHA:3411Down syndrome
ORPHA:870EAST syndrome
ORPHA:199343Ectrodactyly-cleft palate syndrome
ORPHA:1889EEC syndrome
ORPHA:1896EEM syndrome
ORPHA:1897Endocrine-cerebro-osteodysplasia syndrome
ORPHA:199332Epidermolysis bullosa simplex with anodontia/hypodontia
ORPHA:2325Epilepsy with myoclonic-atonic seizures
ORPHA:1942Erythrokeratodermia-cardiomyopathy syndrome
ORPHA:476096Facial dysmorphism-immunodeficiency-livedo-short stature syndrome
ORPHA:352712Febrile infection-related epilepsy syndrome
ORPHA:163703Feingold syndrome
ORPHA:1305GAPO syndrome
ORPHA:2067Global developmental delay-lung cysts-overgrowth-Wilms tumor syndrome
ORPHA:404476GMS 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:306741HNF1B-related autosomal dominant tubulointerstitial kidney disease
ORPHA:93111Holmes-Adie syndrome
ORPHA:454718Holoprosencephaly-craniosynostosis syndrome
ORPHA:2163Hyperinsulinism-hyperammonemia syndrome
ORPHA:35878Hyperornithinemia-hyperammonemia-homocitrullinuria syndrome
ORPHA:415Hypertelorism-microtia-facial clefting syndrome
ORPHA:2213Hyperzincemia and hypercalprotectinemia
ORPHA:251523Hypohidrotic 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:324999Kabuki syndrome
ORPHA:2322Kahrizi syndrome
ORPHA:168972KAT6-related intellectual disability-craniofacial anomalies-cardiac defects syndrome
ORPHA:457193KBG syndrome
ORPHA:2332Keipert syndrome
ORPHA:2662Kenny-Caffey syndrome
ORPHA:2333Keratosis linearis-ichthyosis congenita-sclerosing keratoderma syndrome
ORPHA:281201Keutel syndrome
ORPHA:85202KID syndrome
ORPHA:477Kindler epidermolysis bullosa
ORPHA:2908