Dermis tumor

Summary

Dermis tumor (MONDO:0002300) is a cancer (an umbrella term covering 8 Mondo subtypes). A subtype of skin neoplasm — broader associated-gene and molecular evidence is on the parent page (see Disease family below).

At a glance

• Classification: Cancer
• Umbrella term: 8 Mondo subtypes

Clinical features

No curated clinical features (Orphanet) for this disease.

Identifiers

Disease identifiers

Field	Value
Canonical name	dermis tumor
Mondo ID	MONDO:0002300
DOID	DOID:2438
NCIT	C4475
UMLS	C0346041
MedGen	91075
GARD	0023112
Anatomy (UBERON)	UBERON:0002067
Is cancer (heuristic)	yes

Also known as: dermal neoplasm · dermal tumor · dermal tumour · dermis neoplasm · dermis neoplasm (disease) · dermis tumor · neoplasm of dermis · neoplasm of the dermis · tumor of dermis · tumor of the dermis · tumour of the dermis

Disease family

This is a subtype of skin 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 › skin neoplasm › dermis tumor

Related subtypes (16): dermoid cyst of skin, eyelid neoplasm, epidermal appendage tumor, skin cancer, benign dermal neurilemmoma, actinic keratosis, familial Dupuytren contracture, schwannomatosis, familial multiple discoid fibromas, Maffucci syndrome, hemangiopericytoma of skin, benign neoplasm of skin, melanocytic skin neoplasm, epithelial skin neoplasm, calcifying epithelial odontogenic tumor, familial hyperphosphatemic tumoral calcinosis/hyperphosphatemic hyperostosis syndrome

Subtypes (8): cutaneous granular cell tumor, skin glomus tumor, leiomyoma cutis, malignant dermis tumor, cutaneous fibrous histiocytoma, juvenile hyaline fibromatosis, cutaneous mastocytosis, angioma serpiginosum

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.