Albright's hereditary osteodystrophy

Summary

DOID:0080053 - Albright's hereditary osteodystrophy

Disease Ontology Definition:An pseudohypoparathyroidism 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.

Synonyms: Albright hereditary osteodystrophy, pseudohypoparathyroidism type 1a,

Xenbase Genes Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

: gnas

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0007078 - pseudohypoparathyroidism type 1A

MONDO:0007078 - pseudohypoparathyroidism type 1A

Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Parent(s): pseudohypoparathyroidism (is_a)