Cytomegalovirus pneumonia

Summary

Cytomegalovirus pneumonia (MONDO:0024354) is a disease and 1 clinical trial. A subtype of cytomegalovirus infection — broader associated-gene and molecular evidence is on the parent page (see Disease family below).

At a glance

• Clinical trials: 1

Clinical features

No curated clinical features (Orphanet) for this disease.

Identifiers

Disease identifiers

Field	Value
Canonical name	cytomegalovirus pneumonia
Mondo ID	MONDO:0024354
NCIT	C35360
SNOMED CT	7678002
UMLS	C0276253
MedGen	124443
Is cancer (heuristic)	no

Also known as: CMV pneumonia · Cytomegaloviral pneumonia · Cytomegalovirus caused pneumonia · Cytomegalovirus pneumonia · cytomegalovirus pneumonia

Disease family

This is a subtype of cytomegalovirus infection. 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 etiologic mechanism › disease of primarily extrinsic mechanism › infectious disease › viral infectious disease › primary viral infectious disease › Herpesviridae infectious disease › cytomegalovirus infection › cytomegalovirus pneumonia

Related subtypes (3): cytomegalovirus retinitis, fetal cytomegalovirus syndrome, idiopathic disseminated cytomegalovirus infection

Subtypes (1): cytomegalovirus pneumonia due to NOS2 deficiency

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: 1.

Phase distribution (across all retrieved trials)

Phase	Trials
Not specified	1

Top trials by phase / activity

NCT	Phase	Status	Title
NCT07015801	Not specified	ACTIVE_NOT_RECRUITING	CMV-specific Donor-derived T Lymphocytes for the Treatment of Recalcitrant CMV Infection in a Patient With Primary Immunodeficiency