Facial dysmorphism-ocular anomalies-osteopenia-intellectual disability-dental anomalies syndrome
ORPHA:314555Focal dermal hypoplasia
ORPHA:2092Frontofacionasal dysplasia
ORPHA:1791GAPO syndrome
ORPHA:2067Gardner syndrome
ORPHA:79665Generalized eruptive keratoacanthoma
ORPHA:411777German syndrome
ORPHA:2077Ghosal hematodiaphyseal dysplasia
ORPHA:1802Glaucoma-ectopia lentis-microspherophakia-stiff joints-short stature syndrome
ORPHA:2084Global developmental delay-lung cysts-overgrowth-Wilms tumor syndrome
ORPHA:404476Glossopalatine ankylosis
ORPHA:141163GMS syndrome
ORPHA:2090Goodman syndrome
ORPHA:65798Gordon syndrome
ORPHA:376Gorham-Stout disease
ORPHA:73Gorlin syndrome
ORPHA:377Gorlin-Chaudhry-Moss syndrome
ORPHA:2095GRACILE syndrome
ORPHA:53693Graham Little-Piccardi-Lassueur syndrome
ORPHA:505Grange syndrome
ORPHA:79094Grant syndrome
ORPHA:2097Gray platelet syndrome
ORPHA:721Griscelli syndrome
ORPHA:381Grisel syndrome
ORPHA:662255H syndrome
ORPHA:168569Hajdu-Cheney syndrome
ORPHA:955HEC syndrome
ORPHA:2119Hemiconvulsion-hemiplegia-epilepsy syndrome
ORPHA:86908Holoprosencephaly-craniosynostosis syndrome
ORPHA:2163Hyperornithinemia-hyperammonemia-homocitrullinuria syndrome
ORPHA:415Hypertelorism-microtia-facial clefting syndrome
ORPHA:2213Hypomyelination-hypogonadotropic hypogonadism-hypodontia syndrome
ORPHA:88637Hypoparathyroidism-sensorineural deafness-renal disease syndrome
ORPHA:2237IBIDS syndrome
ORPHA:453ICF syndrome
ORPHA:2268Infantile-onset spinocerebellar ataxia
ORPHA:1186Intellectual disability-eye abnormalities-microcephaly-peripheral spasticity syndrome
ORPHA:404473Iridocorneal endothelial syndrome
ORPHA:64734Isolated congenital onychodysplasia
ORPHA:79144JMP syndrome
ORPHA:324999Joubert syndrome with hepatic defect
ORPHA:1454Junctional epidermolysis bullosa with pyloric atresia
ORPHA:79403KBG syndrome
ORPHA:2332KID syndrome
ORPHA:477L1 syndrome
ORPHA:275543Laryngo-onycho-cutaneous syndrome
ORPHA:2407Mammary-digital-nail syndrome
ORPHA:238744Mandibular hypoplasia-deafness-progeroid features-lipodystrophy syndrome
ORPHA:363649