OBO ID: DOID:0060870
Term Name: isolated growth hormone deficiency Search Ontology:
Synonyms:
  • 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:
  • 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 )
Relationships
is a type of:
has subtype:
OTHER isolated growth hormone deficiency PAGES
GENES INVOLVED No data available
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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