Agranulocytosis
diseaseOn 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
| Field | Value |
|---|---|
| Canonical name | agranulocytosis |
| Mondo ID | MONDO:0001609 |
| MeSH | D000380 |
| DOID | DOID:12987 |
| ICD-10-CM | D70 |
| ICD-11 | 1913706366 |
| NCIT | C2863 |
| SNOMED CT | 417672002 |
| UMLS | C0001824 |
| MedGen | 7932 |
| 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 disorder › leukocyte disorder › leukopenia › agranulocytosis
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)
| Phase | Trials |
|---|---|
| Not specified | 6 |
| PHASE2/PHASE3 | 1 |
Top trials by phase / activity
| NCT | Phase | Status | Title |
|---|---|---|---|
| NCT06707051 | PHASE2/PHASE3 | COMPLETED | Effect of Tranexamic Acid and Calcium Dobesilate for Bleeding of Endometrial Origin |
| NCT00005302 | Not specified | COMPLETED | Drug Etiology of Aplastic Anemia and Related Dyscrasias |
| NCT00005307 | Not specified | COMPLETED | Etiology of Blood Dyscrasias: Analysis of the International Agranulocytosis and Aplastic Anemia Study Data |
| NCT00059423 | Not specified | COMPLETED | Natural History Study for BEN |
| NCT01977963 | Not specified | UNKNOWN | Genetic Study of Antithyroid Drugs Associated Agranulocytosis |
| NCT05349383 | Not specified | COMPLETED | Evaluation of Reporting of Antibody-Drug Conjugate Associated Sepsis-related Toxicities |
| NCT06610500 | Not specified | COMPLETED | Clozapine Hematological Monitoring Regulatory Compliance Assessment in Psychiatry |
Drugs tested across these trials (top 30)
| Molecule | Max phase | Trials referencing |
|---|---|---|
| TRANEXAMIC ACID | 4 | 1 |
Related Atlas pages
- Drugs: Tranexamic Acid