Disease-gene associations mined from literature

Human genes for frontotemporal dementia

Frontotemporal dementia [DOID:9255]

An amino acid metabolic disorder that involves a deficiency of one of the enzymes in the urea cycle which is responsible for removing ammonia from the blood stream.

Synonyms:  frontotemporal dementia,  DOID:9255,  frontotemporal lobar degeneration,  multiple system tauopathy with presenile dementia,  pallidopontonigral degeneration ...

Linkouts:  OMIM #1 #2