Necrosis of pituitary

Summary

Necrosis of pituitary (MONDO:0002721) is a disease. A subtype of pituitary gland disorder — broader associated-gene and molecular evidence is on the parent page (see Disease family below).

Clinical features

No curated clinical features (Orphanet) for this disease.

Identifiers

Disease identifiers

Field	Value
Canonical name	necrosis of pituitary
Mondo ID	MONDO:0002721
DOID	DOID:3646
NCIT	C27066
SNOMED CT	59572000
UMLS	C0271558
MedGen	124404
Is cancer (heuristic)	no

Also known as: pituitary gland Necrosis · pituitary necrosis

Disease family

This is a subtype of pituitary gland disorder. Genetic, therapeutic, and trial evidence is largely curated at the broader-term level — see the parent page for the associated-gene cohort and molecular evidence.

Classification path: disease › human disease › disease by body system or component › reproductive system disorder › pituitary gland disorder › necrosis of pituitary

Related subtypes (8): pituitary hypoplasia, hypopituitarism, empty sella syndrome, inappropriate ADH syndrome, neurohypophyseal diabetes insipidus, pituitary tumor, hypophysitis, anterior pituitary gland disorder

Subtypes (1): pituitary gland infarction

Genetics & variants

GWAS landscape

No GWAS associations recorded — common-variant (GWAS) studies don’t cover this disease (typical for Mendelian / rare diseases). See the curated gene cohort and Mendelian overlap below.

Variant details and genetic-evidence tiers

No tiered GWAS variants or ClinVar records for this disease.

Genes & proteins

No associated-gene cohort resolved for this disease. Atlas builds the molecular and therapeutic sections — associated genes, protein families, druggability, pathways, interactions, and drug associations — by aggregating over a disease’s associated genes (resolved via GWAS / GenCC / ClinVar / CIViC), and none resolved here. This is expected for antibody-mediated, autoimmune, or otherwise non-gene-defined conditions; the curated evidence for this disease is its clinical features, GWAS susceptibility, and clinical trials (above).

Function

No pathway enrichment — requires an associated-gene cohort.

Therapeutics

No druggable-target or therapeutic data for this disease’s cohort.

Clinical trials & evidence

Clinical trials

Clinical trials: 0.