Cutaneous granular cell tumor
disease diseaseOn this page
Also known as cutaneous granular cell neoplasmgranular cell neoplasm of skingranular cell neoplasm of the skingranular cell skin tumorgranular cell skin tumourgranular cell tumor of skingranular cell tumor of the skingranular cell tumor of zone of skingranular cell tumour of the skingranular cell tumour of zone of skinskin granular cell neoplasmskin granular cell tumourzone of skin granular cell tumorzone of skin granular cell tumour
Summary
Cutaneous granular cell tumor (MONDO:0002291) is a cancer. A subtype of dermis 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 | cutaneous granular cell tumor |
| Mondo ID | MONDO:0002291 |
| DOID | DOID:2410 |
| NCIT | C5617 |
| SNOMED CT | 254763007 |
| UMLS | C0346060 |
| MedGen | 138035 |
| GARD | 0023107 |
| Anatomy (UBERON) | UBERON:0000014 |
| Is cancer (heuristic) | yes |
Also known as: cutaneous granular cell neoplasm · cutaneous granular cell tumor · granular cell neoplasm of skin · granular cell neoplasm of the skin · granular cell skin tumor · granular cell skin tumour · granular cell tumor of skin · granular cell tumor of the skin · granular cell tumor of zone of skin · granular cell tumour of the skin · granular cell tumour of zone of skin · skin granular cell neoplasm · skin granular cell tumour · zone of skin granular cell tumor · zone of skin granular cell tumour
Disease family
This is a subtype of dermis 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 etiologic mechanism › cancer or benign tumor › neoplastic disease or syndrome › neoplasm › skin neoplasm › dermis tumor › cutaneous granular cell tumor
Related subtypes (7): skin glomus tumor, leiomyoma cutis, malignant dermis tumor, cutaneous fibrous histiocytoma, juvenile hyaline fibromatosis, cutaneous mastocytosis, angioma serpiginosum
Subtypes (1): malignant cutaneous granular cell skin 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.