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| Term | isolated growth hormone deficiency | ID (Ontology) | DOID:0060870 (Human Disease) |
| Definition | A hypopituitarism characterized by abnormally low levels, absence or impaired function of growth hormone in the absence of abnormalities in other pituitary hormones. | ||
| Also Known As | "congenital IGHD" ; "congenital isolated GH deficiency" ; "congenital isolated growth hormone deficiency" (for all, see Synonyms field below) | ||
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pituitary gland disease |__hypopituitarism |__isolated growth hormone deficiency 2 rec. |__isolated growth hormone deficiency type IA |__isolated growth hormone deficiency type IB 1 rec. |__isolated growth hormone deficiency type II |__isolated growth hormone deficiency type III 1 rec. |
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| Is a | hypopituitarism | ||
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GARD:12556 ICD10CM:E23.0 ICD9CM:253.3 MESH:D004393 NCI:C34555 ORDO:631 SNOMEDCT_US_2025_09_01:270485009 UMLS_CUI:C0013338 |
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