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Disease Ontology Browser
isolated growth hormone deficiency (DOID:0060870)
Alliance: disease page
Synonyms: congenital IGHD; congenital isolated GH deficiency; congenital isolated growth hormone deficiency; familial isolated growth hormone deficiency; IGHD; non-acquired isolated growth hormone deficiency
Alt IDs: ICD10CM:E23.0, ICD9CM:253.3, MESH:D004393, NCI:C34555, ORDO:631, UMLS_CUI:C0013338
Definition: A hypopituitarism characterized by abnormally low levels, absence or impaired function of growth hormone in the absence of abnormalities in other pituitary hormones.

Disease References using Mouse Models (3)

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
03/30/2021
MGI 6.16
The Jackson Laboratory