Craniosynostosis-anal anomalies-porokeratosis syndrome
ORPHA:85199Curly 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:870Ectrodactyly-cleft palate syndrome
ORPHA:1889EEC syndrome
ORPHA:1896EEM syndrome
ORPHA:1897Endocrine-cerebro-osteodysplasia syndrome
ORPHA:199332Erythrokeratodermia-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: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:2119Helsmoortel-Van der Aa syndrome
ORPHA:404448Hemiconvulsion-hemiplegia-epilepsy syndrome
ORPHA:86908Hemidystonia-hemiatrophy syndrome
ORPHA:306741Hemiparkinsonism-hemiatrophy syndrome
ORPHA:306669HNF1B-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: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:2268Ichthyosis-hypotrichosis syndrome
ORPHA:91132Iridocorneal endothelial syndrome
ORPHA:64734JMP syndrome
ORPHA:324999KBG syndrome
ORPHA:2332KID syndrome
ORPHA:477L1 syndrome
ORPHA:275543Laryngo-onycho-cutaneous syndrome
ORPHA:2407