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 )
Relationships
Other Pages
Genes Involved
Zebrafish Models