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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 (3)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
08/08/2017
MGI 6.10
The Jackson Laboratory