Cervical lymphadenitis

Summary

Cervical lymphadenitis (MONDO:0003067) is a disease. A subtype of lymphadenitis — 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	cervical lymphadenitis
Mondo ID	MONDO:0003067
DOID	DOID:4637
NCIT	C26937
SNOMED CT	3502005
UMLS	C0149642
MedGen	101763
Anatomy (UBERON)	UBERON:0000974
Is cancer (heuristic)	no

Also known as: lymphadenitis (disease) of neck · neck lymphadenitis (disease)

Disease family

This is a subtype of lymphadenitis. 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 › immune system disorder › lymphoid system disorder › lymphatic system disorder › lymph node disorder › lymphadenitis › cervical lymphadenitis

Related subtypes (9): mesenteric lymphadenitis, postauricular lymphadenitis, suppurative lymphadenitis, axillary lymphadenitis, cat-scratch disease, sialadenitis, Kawasaki disease, Kimura disease, Kikuchi-Fujimoto disease

Subtypes (1): submandibular adenitis

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.