Chronic sphenoidal sinusitis

disease
On this page

Also known as chronic sphenoid sinusitissphenoid sinusitis, chronic

Summary

Chronic sphenoidal sinusitis (MONDO:0001123) is a disease. A subtype of sphenoid sinusitis — 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

FieldValue
Canonical namechronic sphenoidal sinusitis
Mondo IDMONDO:0001123
DOIDDOID:10793
ICD-10-CMJ32.3
ICD-11627227610
NCITC34480
SNOMED CT38961000
UMLSC0008712
MedGen3087
Is cancer (heuristic)no

Also known as: chronic sphenoid sinusitis · sphenoid sinusitis, chronic

Disease family

This is a subtype of sphenoid sinusitis. 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 diseasenasal disorderparanasal sinus disordersinusitissphenoid sinusitischronic sphenoidal sinusitis

Related subtypes (1): acute sphenoidal sinusitis

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.

No linked Atlas pages yet — the cross-entity mesh grows as the corpus expands.