Orbit embryonal rhabdomyosarcoma

Summary

Orbit embryonal rhabdomyosarcoma (MONDO:0002579) is a disease. A subtype of orbit rhabdomyosarcoma — 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	orbit embryonal rhabdomyosarcoma
Mondo ID	MONDO:0002579
DOID	DOID:3258
NCIT	C6246
UMLS	C1335127
MedGen	233267
GARD	0023173
Is cancer (heuristic)	no

Also known as: embryonal rhabdomyosarcoma of orbit · embryonal rhabdomyosarcoma of the orbit

Disease family

This is a subtype of orbit rhabdomyosarcoma. 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 › musculoskeletal system disorder › musculoskeletal system cancer › bone cancer › skull cancer › orbital cancer › orbit sarcoma › orbit rhabdomyosarcoma › orbit embryonal rhabdomyosarcoma

Related subtypes (1): orbit alveolar rhabdomyosarcoma

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.