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Disease Ontology Browser
pseudohypoparathyroidism (DOID:4184)
Alliance: disease page
Synonyms: PHP
Alt IDs: ICD10CM:E20.1, MESH:D011547, NCI:C99027, UMLS_CUI:C0033806
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.

Disease References using Mouse Models (6)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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last database update
12/17/2024
MGI 6.24
The Jackson Laboratory