frontotemporal dementia with motor neuron disease
http://purl.obolibrary.org/obo/MONDO_0017161
Frontotemporal dementia with motor neuron disease (FTD-MND) is a type of frontotemporal lobar degeneration characterized by the insidious onset (between the ages of 38-78 years) of dementia-associated psychiatric symptoms (e.g. personality changes, uninhibited behavior, irritability, aggressiveness), memory difficulties, global intellectual impairment, emotional disorders and transcortical motor aphasia that eventually leads to mutism, in addition to the manifestations of motor neuron disease such as neurogenic muscular wasting (similar to what is seen in amyotrophic lateral sclerosis). The disease is progressive, with death occurring 2-5 years after onset. [ Orphanet:275872 ]
Term info
- Orphanet:275872 (MONDO:equivalentTo)
- MESH:C566288 (MONDO:equivalentTo)
- OMIMPS:105550 (MONDO:equivalentTo)
- UMLS:CN239493 (MONDO:equivalentTo)
ordo_disease
Frontotemporal dementia with motor neuron disease (FTD-MND) is a type of frontotemporal lobar degeneration characterized by the insidious onset (between the ages of 38-78 years) of dementia-associated psychiatric symptoms (e.g. personality changes, uninhibited behavior, irritability, aggressiveness), memory difficulties, global intellectual impairment, emotional disorders and transcortical motor aphasia that eventually leads to mutism, in addition to the manifestations of motor neuron disease such as neurogenic muscular wasting (similar to what is seen in amyotrophic lateral sclerosis). The disease is progressive, with death occurring 2-5 years after onset.
https://omim.org/phenotypicSeries/PS105550, http://purl.obolibrary.org/obo/Orphanet_275872, http://identifiers.org/mesh/C566288, http://linkedlifedata.com/resource/umls/id/CN239493
FTDALS, FTD-MND, frontotemporal dementia with amyotrophic lateral sclerosis, frontotemporal dementia with ALS, FTD-ALS
MONDO:0017161