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Summary Literature (0)
DOID:0080053 - Albright's hereditary osteodystrophy


Disease Ontology 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.

Synonyms: Albright hereditary osteodystrophy, pseudohypoparathyroidism type 1a

In OMIM:
OMIM:103580 - PSEUDOHYPOPARATHYROIDISM, TYPE IA; PHP1A

In Mondo Disease Ontology:
MONDO:0007078 - pseudohypoparathyroidism type 1A

Human Disease Resources: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Xenbase Genes : gnas

Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Parent(s): pseudohypoparathyroidism (is_a)