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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
Echinobase Genes
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| OMIM:103580 - pseudohypoparathyroidism, type ia; php1a |
Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
pseudohypoparathyroidism (is_a)