FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
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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Synonyms
  • "congenital IGHD" EXACT
    "congenital isolated GH deficiency" EXACT
    "congenital isolated growth hormone deficiency" EXACT
    "familial isolated growth hormone deficiency" EXACT
    "IGHD" EXACT OMO:0003012
    "non-acquired isolated growth hormone deficiency" EXACT
Secondary IDs
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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