Orbital myositis

Summary

Orbital myositis (MONDO:0100550) is a disease. A subtype of myopathy of extraocular muscle — 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	orbital myositis
Mondo ID	MONDO:0100550
ICD-10-CM	H05.12
NCIT	C117296
SNOMED CT	80698001
UMLS	C2350476
MedGen	389999
GARD	0026276
Anatomy (UBERON)	UBERON:0001601
Is cancer (heuristic)	no

Also known as: ocular myositis

Disease family

This is a subtype of myopathy of extraocular muscle. 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 › disorder of orbital region › eye adnexa disorder › myopathy of extraocular muscle › orbital myositis

Related subtypes (2): congenital fibrosis of extraocular muscles, oculopharyngeal muscular dystrophy

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.