Alkhurma hemorrhagic fever

Summary

Alkhurma hemorrhagic fever (MONDO:0000310) is a disease. A subtype of Kyasanur forest disease — 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	Alkhurma hemorrhagic fever
Mondo ID	MONDO:0000310
DOID	DOID:0050308
UMLS	C5230236
MedGen	1684673
GARD	0022744
Is cancer (heuristic)	no

Also known as: Alkhumra hemorrhagic fever virus caused disease or disorder · Alkhumra hemorrhagic fever virus disease or disorder · Alkhumra hemorrhagic fever virus infectious disease

Disease family

Classification path: disease › human disease › disease by etiologic mechanism › disease of primarily extrinsic mechanism › infectious disease › viral infectious disease › primary viral infectious disease › Flaviviridae infectious disease › Kyasanur forest disease › Alkhurma hemorrhagic fever

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.