Mediastinal granular cell myoblastoma
disease diseaseOn this page
Also known as granular cell myoblastoma of mediastinumgranular cell myoblastoma of the mediastinumgranular cell neoplasm of mediastinumgranular cell neoplasm of the mediastinumgranular cell tumor of mediastinumgranular cell tumor of the mediastinumgranular cell tumour of mediastinumgranular cell tumour of the mediastinummediastinal granular cell neoplasmmediastinal granular cell tumormediastinal granular cell tumourmediastinum granular cell tumormediastinum granular cell tumour
Summary
Mediastinal granular cell myoblastoma (MONDO:0003255) is a disease. A subtype of granular cell tumor — 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 | mediastinal granular cell myoblastoma |
| Mondo ID | MONDO:0003255 |
| DOID | DOID:5046 |
| NCIT | C6601 |
| UMLS | C1334656 |
| MedGen | 235309 |
| GARD | 0023426 |
| Anatomy (UBERON) | UBERON:0003728 |
| Is cancer (heuristic) | no |
Also known as: granular cell myoblastoma of mediastinum · granular cell myoblastoma of the mediastinum · granular cell neoplasm of mediastinum · granular cell neoplasm of the mediastinum · granular cell tumor of mediastinum · granular cell tumor of the mediastinum · granular cell tumour of mediastinum · granular cell tumour of the mediastinum · mediastinal granular cell myoblastoma · mediastinal granular cell neoplasm · mediastinal granular cell tumor · mediastinal granular cell tumour · mediastinum granular cell tumor · mediastinum granular cell tumour
Disease family
This is a subtype of granular cell tumor. 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 › nervous system disorder › peripheral nervous system disorder › peripheral nervous system neoplasm › nerve sheath neoplasm › granular cell tumor › mediastinal granular cell myoblastoma
Related subtypes (8): cutaneous granular cell tumor, breast granular cell tumor, benign granular cell tumor, esophageal granular cell tumor, granular cell cancer, vulvar granular cell tumor, neurohypophysis granular cell tumor, congenital epulis
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.