Cardiac granular cell neoplasm
disease diseaseOn this page
Also known as Cardiac granular cell tumorCardiac granular cell tumourgranular cell neoplasm of heartgranular cell neoplasm of the heartgranular cell tumor of heartgranular cell tumor of the heartgranular cell tumour of heartgranular cell tumour of the heartheart granular cell tumorheart granular cell tumour
Summary
Cardiac granular cell neoplasm (MONDO:0003254) is a cancer. A subtype of benign granular cell tumor — 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 | cardiac granular cell neoplasm |
| Mondo ID | MONDO:0003254 |
| DOID | DOID:5044 |
| NCIT | C5360 |
| UMLS | C1332845 |
| MedGen | 232023 |
| GARD | 0023425 |
| Anatomy (UBERON) | UBERON:0000948 |
| Is cancer (heuristic) | yes |
Also known as: Cardiac granular cell neoplasm · Cardiac granular cell tumor · Cardiac granular cell tumour · granular cell neoplasm of heart · granular cell neoplasm of the heart · granular cell tumor of heart · granular cell tumor of the heart · granular cell tumour of heart · granular cell tumour of the heart · heart granular cell tumor · heart granular cell tumour
Disease family
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 › benign granular cell tumor › cardiac granular cell neoplasm
Related subtypes (1): benign peripheral nerve granular cell tumor
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.