Search Ontology:
Human Disease
isolated growth hormone deficiency
- Term ID
- DOID:0060870
- Synonyms
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- congenital IGHD
- congenital isolated GH deficiency
- congenital isolated growth hormone deficiency
- familial isolated growth hormone deficiency
- IGHD
- non-acquired isolated growth hormone deficiency
- Definition
- A hypopituitarism characterized by abnormally low levels, absence or impaired function of growth hormone in the absence of abnormalities in other pituitary hormones. https://www.ncbi.nlm.nih.gov/pubmed/8288694
- References
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- GARD:12556
- ICD10CM:E23.0
- ICD9CM:253.3
- MESH:D004393
- NCI:C34555
- ORDO:631
- SNOMEDCT_US_2023_03_01:270485009
- UMLS_CUI:C0013338
- Ontology
- Human Disease ( DOID:0060870 )
- is a type of
-
- has subtype
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Other Pages
Genes Involved
Zebrafish Models