Multi-infarct dementia
diseaseOn this page
Also known as Binswanger diseaseBinswanger's diseasedementia multi infarctdementia multi-infarctdementia multi-infarctsdementia, lacunardementia, multi infarctdementia, MultiinfarctDementias, lacunarDementias, multi-infarctDementias, Multiinfarctlacunar dementialacunar Dementiasmulti infarct dementiamulti-infarct Dementiasmulti-infarct, dementiamulti-infarcts, dementiaMultiinfarct dementiaMultiinfarct Dementias
Summary
Multi-infarct dementia (MONDO:0043224) is a disease and 4 clinical trials. A subtype of cerebral infarction — broader associated-gene and molecular evidence is on the parent page (see Disease family below).
At a glance
- Clinical trials: 4
Clinical features
No curated clinical features (Orphanet) for this disease.
Identifiers
Disease identifiers
| Field | Value |
|---|---|
| Canonical name | multi-infarct dementia |
| Mondo ID | MONDO:0043224 |
| MeSH | D015161 |
| ICD-11 | 645643099 |
| NCIT | C34522 |
| SNOMED CT | 56267009 |
| UMLS | C0011263 |
| MedGen | 8277 |
| Is cancer (heuristic) | no |
Also known as: Binswanger disease · Binswanger’s disease · dementia multi infarct · dementia multi-infarct · dementia multi-infarcts · dementia, lacunar · dementia, multi infarct · dementia, Multiinfarct · Dementias, lacunar · Dementias, multi-infarct · Dementias, Multiinfarct · lacunar dementia · lacunar Dementias · multi infarct dementia · multi-infarct dementia · multi-infarct Dementias · multi-infarct, dementia · multi-infarcts, dementia · Multiinfarct dementia · Multiinfarct Dementias
Disease family
This is a subtype of cerebral infarction. 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 › nervous system disorder › central nervous system disorder › brain disorder › cerebrovascular disorder › brain infarction › cerebral infarction › multi-infarct dementia
Related subtypes (3): anterior cerebral artery infarction, middle cerebral artery infarction, posterior cerebral artery infarction
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: 4.
Phase distribution (across all retrieved trials)
| Phase | Trials |
|---|---|
| Not specified | 4 |
Top trials by phase / activity
| NCT | Phase | Status | Title |
|---|---|---|---|
| NCT03724136 | Not specified | UNKNOWN | Alzheimer’s Autism and Cognitive Impairment Stem Cell Treatment Study |
| NCT04165213 | Not specified | COMPLETED | Care of Persons With Dementia in Their Environments (COPE) in Programs of All-Inclusive Care of the Elderly (PACE) |
| NCT04428112 | Not specified | COMPLETED | Rural Dementia Caregiver Project |
| NCT04828434 | Not specified | UNKNOWN | Virtual Individual Cognitive Stimulation Therapy: a Proof of Concept Study |
Related Atlas pages
No linked Atlas pages yet — the cross-entity mesh grows as the corpus expands.