Glycogen storage disease due to phosphoglycerate kinase 1 deficiency

X-linked recessive

Adolescent, Adult, Childhood

Glycogen storage disease due to phosphoglycerate mutase deficiency

Autosomal recessive

Adolescent, Childhood

Glycogen storage disease due to phosphorylase kinase deficiency

Autosomal recessive, X-linked recessive

All ages

Glycogen storage disease with severe cardiomyopathy due to glycogenin deficiency

Autosomal recessive

Childhood

Gnathodiaphyseal dysplasia

Autosomal dominant

Adolescent, Childhood, Infancy

Goblet cell carcinoma

Not applicable

Adult

Goldberg-Shprintzen megacolon syndrome

Autosomal recessive

Infancy, Neonatal

Goldmann-Favre syndrome

Autosomal recessive

Adolescent, Childhood

Gollop-Wolfgang complex

Autosomal dominant, Autosomal recessive

Antenatal, Neonatal

Gonadoblastoma

Adolescent

Gonococcal conjunctivitis

All ages

Gordon syndrome

Autosomal dominant

Antenatal, Neonatal

Gorham-Stout disease

Not applicable

All ages

Gorlin syndrome

Autosomal dominant

Adolescent, Adult

Gorlin-Chaudhry-Moss syndrome

Autosomal recessive

Neonatal

Graft versus host disease

Not applicable

All ages

Graham Little-Piccardi-Lassueur syndrome

Adult

Grange syndrome

Autosomal dominant, Autosomal recessive

Childhood

Grant syndrome

Unknown

Neonatal

Granular corneal dystrophy type I

Autosomal dominant

Childhood

Granular corneal dystrophy type II

Autosomal dominant

Childhood

Granulomatosis with polyangiitis

Not applicable

Adolescent, Adult, Childhood, Elderly

Granulomatous mastitis

Adolescent, Adult, Elderly

Granulomatous slack skin

Not applicable

Adult