Search Ontology:
Human Disease
frontotemporal dementia 1
- Term ID
- DOID:0051060
- Synonyms
-
- Definition
- A frontotemporal dementia that has_material_basis_in heterozygous mutation in the MAPT gene, which encodes microtubule-associated protein tau, on chromosome 17q21. https://www.ncbi.nlm.nih.gov/books/NBK1505/
- References
- Ontology
- Human Disease ( DOID:0051060 )
Other Pages
Genes Involved
Zebrafish Models