Blackwater fever

Summary

Blackwater fever (MONDO:0005670) is a disease. A subtype of malaria — 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	blackwater fever
Mondo ID	MONDO:0005670
EFO	EFO:0007172
MeSH	D001742
DOID	DOID:14068
NCIT	C34426
SNOMED CT	56625005
UMLS	C0005681
MedGen	2277
GARD	0024215
Is cancer (heuristic)	no

Also known as: blackwater fever · malarial hemoglobinuria

Disease family

This is a subtype of malaria. 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 › parasitic infectious disease › protozoa infectious disease › malaria › blackwater fever

Related subtypes (6): Plasmodium ovale malaria, Plasmodium malariae malaria, mixed malaria, cerebral malaria, Plasmodium falciparum malaria, Plasmodium vivax malaria

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.