Maxillary sinus cholesteatoma

Summary

Maxillary sinus cholesteatoma (MONDO:0006577) is a disease. A subtype of paranasal sinus disorder — 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	maxillary sinus cholesteatoma
Mondo ID	MONDO:0006577
DOID	DOID:867
NCIT	C35868
UMLS	C1334644
MedGen	277346
Anatomy (UBERON)	UBERON:0001764
Is cancer (heuristic)	no

Also known as: cholesteatoma (disease) of maxillary sinus · maxillary sinus cholesteatoma (disease)

Disease family

This is a subtype of paranasal sinus disorder. 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 › otorhinolaryngologic disease › nasal disorder › paranasal sinus disorder › maxillary sinus cholesteatoma

Related subtypes (6): paranasal sinus neoplasm, sinusitis, polyp of sphenoidal sinus, polyp of frontal sinus, polyp of maxillary sinus, polyp of ethmoidal sinus

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.