Panhypopituitarism

Preferred Label : Panhypopituitarism;

ICD-11 definition : A clinical status with impaired synthesis/secretion of all six anterior pituitary hormones caused by a variety of tumorous and non-tumorous diseases, manifesting i secondary hypoadrenocorticism, hypothyroidism, and hypognadotropic hypogonadism.;

Details

Origin ID

1576287890;

Automatic exact mappings (from CISMeF team)
- Hypopituitarism [ICD-10 Sub-category]
- Non-acquired panhypopituitarism [ORDO Disease]
- Panhypopituitarism [NCIt concept]
- Panhypopituitarism [PASCAL descriptor]
- Panhypopituitarism [MedDRA LLT]
- Panhypopituitarism [ICD-9 code]
- Panhypopituitarism [HPO term]
- Panhypopituitarism (disorder) [SNOMED CT concept]
- Pituitary hormone deficiency, combined, 2 [OMIM Phenotype]
- SRY-box transcription factor 3 [ORDO Gene]
- combined pituitary hormone deficiency [MeSH Supplementary Concept]
- panhypopituitarism [DO Concept]
- panhypopituitarism, nos [SNOMED Notion]
Validated automatic mappings to BTNT
- hypopituitarism [MeSH Descriptor]

Keyword's position in hierarchy(ies) :

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