Agranulocytosis

disease
On this page

Also known as granulocytopenia

Summary

Agranulocytosis (MONDO:0001609) is a disease and 7 clinical trials. Top therapeutic interventions include tranexamic acid. A subtype of leukopenia — broader associated-gene and molecular evidence is on the parent page (see Disease family below).

At a glance

  • Clinical trials: 7

Clinical features

No curated clinical features (Orphanet) for this disease.

Identifiers

Disease identifiers

FieldValue
Canonical nameagranulocytosis
Mondo IDMONDO:0001609
MeSHD000380
DOIDDOID:12987
ICD-10-CMD70
ICD-111913706366
NCITC2863
SNOMED CT417672002
UMLSC0001824
MedGen7932
Is cancer (heuristic)no

Also known as: granulocytopenia

Disease family

This is a subtype of leukopenia. 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 disorderleukocyte disorderleukopeniaagranulocytosis

Related subtypes (1): lymphopenia

Subtypes (2): neutropenia, acquired agranulocytosis

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: 7.

Phase distribution (across all retrieved trials)

PhaseTrials
Not specified6
PHASE2/PHASE31

Top trials by phase / activity

NCTPhaseStatusTitle
NCT06707051PHASE2/PHASE3COMPLETEDEffect of Tranexamic Acid and Calcium Dobesilate for Bleeding of Endometrial Origin
NCT00005302Not specifiedCOMPLETEDDrug Etiology of Aplastic Anemia and Related Dyscrasias
NCT00005307Not specifiedCOMPLETEDEtiology of Blood Dyscrasias: Analysis of the International Agranulocytosis and Aplastic Anemia Study Data
NCT00059423Not specifiedCOMPLETEDNatural History Study for BEN
NCT01977963Not specifiedUNKNOWNGenetic Study of Antithyroid Drugs Associated Agranulocytosis
NCT05349383Not specifiedCOMPLETEDEvaluation of Reporting of Antibody-Drug Conjugate Associated Sepsis-related Toxicities
NCT06610500Not specifiedCOMPLETEDClozapine Hematological Monitoring Regulatory Compliance Assessment in Psychiatry

Drugs tested across these trials (top 30)

MoleculeMax phaseTrials referencing
TRANEXAMIC ACID41