|  Help  |  About  |  Contact Us

DO Term : pseudohypoparathyroidism [DOID:4184] Disease Ontology

Namespace  disease_ontology Obsolete  false
description  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:
  • UMLS_CUI:C0033806,
  • ICD10CM:E20.1,
  • SNOMEDCT_US_2023_03_01:190867002,
  • GARD:10758,
  • NCI:C99027,
  • PHP,
  • MESH:D011547
Quick Links:
 
Quick Links:
 

Disease

Diseases --> Human genes

Diseases --> Mouse genes

Diseases --> Mouse models

Ontology

Ontology Term --> All ancestors

Ontology Term --> All descendants

Ontology Term --> Direct children

Ontology Term --> Direct parents