About   Help   FAQ
Disease Ontology Browser
Albright's hereditary osteodystrophy (DOID:0080053)
Synonyms: Albright hereditary osteodystrophy; pseudohypoparathyroidism type 1a
Alt IDs: OMIM:103580
Definition: An osteochondrodysplasia that has_material_basis_in lack of responsiveness to parathyroid hormone which results_in shortening and widening of long bones of the located_in hand or located_in foot along with short stature, obesity, and rounded face.

Disease References using Mouse Models (2)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
Citing These Resources
Funding Information
Warranty Disclaimer & Copyright Notice
Send questions and comments to User Support.
last database update
04/18/2017
MGI 6.08
The Jackson Laboratory