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 ...