About   Help   FAQ
Disease Ontology Browser
progeria (DOID:3911)
Alliance: disease page
Synonyms: HGPS; Hutchinson Gilford syndrome; Hutchinson-Gilford disease; Hutchinson-Gilford Progeria syndrome
Alt IDs: OMIM:176670, ICD10CM:E34.8, MESH:D011371, NCI:C34951, ORDO:740, UMLS_CUI:C0033300
Definition: A progeroid 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 the LMNA gene on chromosome 1q22.

Disease References using Mouse Models (31)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support.
last database update
MGI 6.22
The Jackson Laboratory