Transient global amnesia
disease diseaseOn this page
Also known as transient global amnesia (disease)
Summary
Transient global amnesia (MONDO:0001617) is a disease and 5 clinical trials. A subtype of amnestic disorder — broader associated-gene and molecular evidence is on the parent page (see Disease family below).
At a glance
- Clinical trials: 5
Clinical features
No curated clinical features (Orphanet) for this disease.
Identifiers
Disease identifiers
| Field | Value |
|---|---|
| Canonical name | transient global amnesia |
| Mondo ID | MONDO:0001617 |
| MeSH | D020236 |
| DOID | DOID:13027 |
| ICD-10-CM | G45.4 |
| ICD-11 | 1524600518 |
| NCIT | C85198 |
| UMLS | C0338591 |
| MedGen | 83275 |
| GARD | 0027583 |
| Is cancer (heuristic) | no |
Also known as: transient global amnesia · transient global amnesia (disease)
Data availability: 1 HPO phenotype.
Disease family
This is a subtype of amnestic disorder. 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 developmental or physiological process › psychiatric disorder › cognitive disorder › amnestic disorder › transient global amnesia
Related subtypes (3): retrograde amnesia, anterograde amnesia, alcohol amnestic disorder
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: 5.
Phase distribution (across all retrieved trials)
| Phase | Trials |
|---|---|
| Not specified | 5 |
Top trials by phase / activity
| NCT | Phase | Status | Title |
|---|---|---|---|
| NCT01793168 | Not specified | RECRUITING | Rare Disease Patient Registry & Natural History Study - Coordination of Rare Diseases at Sanford |
| NCT06903026 | Not specified | RECRUITING | PRevalence Of Transient Global Amnesia in Obstructive Sleep Apnea Syndrome |
| NCT07009990 | Not specified | NOT_YET_RECRUITING | Coronary and Cerebral Microvascular Dysfunction in Neurological Diseases |
| NCT02562560 | Not specified | TERMINATED | Neuropsycholgy and Neuroimaging in Transient Global Amnesia |
| NCT03739008 | Not specified | COMPLETED | Reversible Cerebral Vasoconstriction Syndrome With Concomitant Transient Global Amnesia |
Related Atlas pages
No linked Atlas pages yet — the cross-entity mesh grows as the corpus expands.