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:1897Emanuel syndrome
ORPHA:96170Endocrine-cerebro-osteodysplasia syndrome
ORPHA:199332Erythrokeratodermia-cardiomyopathy syndrome
ORPHA:476096Facial dysmorphism-immunodeficiency-livedo-short stature syndrome
ORPHA:352712Febrile infection-related epilepsy syndrome
ORPHA:163703Frey syndrome
ORPHA:662240GAPO syndrome
ORPHA:2067GMS syndrome
ORPHA:2090Gorlin-Chaudhry-Moss syndrome
ORPHA:2095Grisel syndrome
ORPHA:662255H syndrome
ORPHA:168569HARP syndrome
ORPHA:157855HEC syndrome
ORPHA:2119Hemiconvulsion-hemiplegia-epilepsy syndrome
ORPHA:86908Hemidystonia-hemiatrophy syndrome
ORPHA:306741Hinman syndrome
ORPHA:84085HNF1B-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:2237IBIDS syndrome
ORPHA:453ICF syndrome
ORPHA:2268Intellectual disability, Buenos-Aires type
ORPHA:3079Iridocorneal endothelial syndrome
ORPHA:64734JMP syndrome
ORPHA:324999KBG syndrome
ORPHA:2332Keutel syndrome
ORPHA:85202KID syndrome
ORPHA:477KLHL7-related Bohring-Opitz-like and Crisponi/Cold-induced sweating-like overlap syndrome
ORPHA:603684L1 syndrome
ORPHA:275543Laryngo-onycho-cutaneous syndrome
ORPHA:2407Lethal ataxia with deafness and optic atrophy
ORPHA:1187Lethal omphalocele-cleft palate syndrome
ORPHA:2736LIG4 syndrome
ORPHA:99812Linear nevus sebaceus syndrome
ORPHA:2612Mammary-digital-nail syndrome
ORPHA:238744Mandibular hypoplasia-deafness-progeroid features-lipodystrophy syndrome
ORPHA:363649