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Echinobase
Summary Literature (0)
DOID:4184 - pseudohypoparathyroidism

Disease Ontology Definition:A metal metabolism disorder that is characterized by end-organ resistance to parathyroid hormone and/or a constellation of symptoms collectively termed Albright’s hereditary osteodystrophy, which include shortening and widening of long bones located_in the hand or located_in the foot along with short stature, obesity, and rounded face.

Synonyms: PHP

Echinobase Genes : stx16


MIM:
MIM:603233 - pseudohypoparathyroidism, type ib; php1b

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

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): metal metabolism disorder (is_a)