|
DOID:0060870 - isolated growth hormone deficiency
Disease Ontology Definition:A hypopituitarism characterized by abnormally low levels, absence or impaired function of growth hormone in the absence of abnormalities in other pituitary hormones.
Synonyms: IGHD, congenital IGHD, congenital isolated GH deficiency, congenital isolated growth hormone deficiency, familial isolated growth hormone deficiency, non-acquired isolated growth hormone deficiency,
Xenbase Genes
![Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries](img/icons/info1.png)
MONDO:0000050 - isolated congenital growth hormone deficiency |
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
hypopituitarism (is_a)