Hantavirus hemorrhagic fever with renal syndrome, Puumala virus type

Summary

Hantavirus hemorrhagic fever with renal syndrome, Puumala virus type (MONDO:0000284) is a disease. A subtype of hantavirus hemorrhagic fever with renal syndrome — 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	Hantavirus hemorrhagic fever with renal syndrome, Puumala virus type
Mondo ID	MONDO:0000284
DOID	DOID:0050201
UMLS	C0242993
MedGen	69308
GARD	0027518
Is cancer (heuristic)	no

Also known as: nephropathis epidemica

Disease family

This is a subtype of hantavirus hemorrhagic fever with renal syndrome. 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 › urinary system disorder › kidney disorder › renal infectious disease › hantavirus hemorrhagic fever with renal syndrome › Hantavirus hemorrhagic fever with renal syndrome, Puumala virus type

Related subtypes (3): Hantavirus hemorrhagic fever with renal syndrome, Seoul virus type, Hantavirus hemorrhagic fever with renal syndrome, Dobrava-Belgrade virus type, BK-virus nephropathy

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.