Double uterus-hemivagina-renal agenesis syndrome
ORPHA:3411Down syndrome
ORPHA:870Ectrodactyly-cleft palate syndrome
ORPHA:1889EEC syndrome
ORPHA:1896EEM syndrome
ORPHA:1897Endocrine-cerebro-osteodysplasia syndrome
ORPHA:199332Erythrokeratodermia-cardiomyopathy syndrome
ORPHA:476096Facial dysmorphism-anorexia-cachexia-eye and skin anomalies syndrome
ORPHA:1969Facial dysmorphism-immunodeficiency-livedo-short stature syndrome
ORPHA:352712Familial atypical multiple mole melanoma syndrome
ORPHA:404560Feingold syndrome
ORPHA:1305Fibular aplasia-complex brachydactyly syndrome
ORPHA:2639Fragile X syndrome
ORPHA:908GAPO syndrome
ORPHA:2067Gingival fibromatosis-progressive deafness syndrome
ORPHA:2027GMS 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 fibrosing poikiloderma-tendon contractures-myopathy-pulmonary fibrosis syndrome
ORPHA:221043Holmes-Adie syndrome
ORPHA:454718Hyperornithinemia-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:2237IBIDS syndrome
ORPHA:453ICF syndrome
ORPHA:2268Intellectual disability-obesity-prognathism-eye and skin anomalies syndrome
ORPHA:397973Iridocorneal endothelial syndrome
ORPHA:64734JMP syndrome
ORPHA:324999Juvenile hyaline fibromatosis
ORPHA:2028KBG syndrome
ORPHA:2332KID syndrome
ORPHA:477L1 syndrome
ORPHA:275543Laryngeal abductor paralysis-intellectual disability syndrome
ORPHA:2375Laryngo-onycho-cutaneous syndrome
ORPHA:2407Lethal ataxia with deafness and optic atrophy
ORPHA:1187LIG4 syndrome
ORPHA:99812LUMBAR syndrome
ORPHA:83628Mammary-digital-nail syndrome
ORPHA:238744Mandibular hypoplasia-deafness-progeroid features-lipodystrophy syndrome
ORPHA:363649MASA syndrome
ORPHA:2466MASS syndrome
ORPHA:99715