Neurohypophysis granular cell tumor
diseaseOn this page
Also known as granular cell tumor of Neurohypophysisgranular cell tumor of the neurohypophysisgranular cell tumor of the Neurohypophysis (WHO grade I)granular cell tumor of the posterior pituitary glandgranular cell tumour of Neurohypophysisgranular cell tumour of the neurohypophysisgranular cell tumour of the Neurohypophysis (WHO grade I)granular cell tumour of the posterior pituitary gland
Summary
Neurohypophysis granular cell tumor (MONDO:0003256) is a cancer. A subtype of posterior pituitary gland neoplasm — broader associated-gene and molecular evidence is on the parent page (see Disease family below).
At a glance
- Classification: Cancer
Clinical features
No curated clinical features (Orphanet) for this disease.
Identifiers
Disease identifiers
| Field | Value |
|---|---|
| Canonical name | neurohypophysis granular cell tumor |
| Mondo ID | MONDO:0003256 |
| EFO | EFO:1000285 |
| DOID | DOID:5047 |
| NCIT | C7017 |
| SNOMED CT | 699331002 |
| UMLS | C1333873 |
| MedGen | 232255 |
| GARD | 0023427 |
| Anatomy (UBERON) | UBERON:0002198 |
| Is cancer (heuristic) | yes |
Also known as: granular cell tumor of Neurohypophysis · granular cell tumor of neurohypophysis · granular cell tumor of the neurohypophysis · granular cell tumor of the Neurohypophysis (WHO grade I) · granular cell tumor of the posterior pituitary gland · granular cell tumour of Neurohypophysis · granular cell tumour of neurohypophysis · granular cell tumour of the neurohypophysis · granular cell tumour of the Neurohypophysis (WHO grade I) · granular cell tumour of the posterior pituitary gland · neurohypophysis granular cell tumor
Disease family
This is a subtype of posterior pituitary gland neoplasm. 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 etiologic mechanism › cancer or benign tumor › neoplastic disease or syndrome › neoplasm › endocrine gland neoplasm › pituitary tumor › posterior pituitary gland neoplasm › neurohypophysis granular cell tumor
Related subtypes (3): pituitary stalk meningioma, pituicytoma, spindle cell oncocytoma
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.
Related Atlas pages
No linked Atlas pages yet — the cross-entity mesh grows as the corpus expands.