DISEASES

Disease-gene associations mined from literature

Human genes for progeria

Progeria [DOID:3911]

A syndrome characterized by extreme short stature, low body weight, early loss of hair, lipodystrophy, scleroderma, decreased joint mobility, osteolysis, and facial features that resemble aged persons that has_material_basis_in mutation in LMNA on chromosome 1q22.

Synonyms:  progeria,  DOID:3911,  progerias,  HGPS,  Hutchinson-Gilford disease ...

Linkouts:  OMIM #1 #2