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frontotemporal dementia with motor neuron disease

Go to external page 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 ]

Synonyms: FTDALS FTD-MND frontotemporal dementia with amyotrophic lateral sclerosis frontotemporal dementia with ALS FTD-ALS

This is just here as a test because I lose it

Term information

database cross reference
  • GARD:17273 (MONDO:GARD)
  • Orphanet:275872 (MONDO:equivalentTo)
  • MESH:C566288 (MONDO:equivalentTo)
  • OMIMPS:105550 (MONDO:equivalentTo)
Subsets

ordo_disorder, gard_rare, otar, rare, nord_rare, orphanet_rare

abbreviation
FTDALS [ MONDO:0000712 ]

exactMatch

https://omim.org/phenotypicSeries/PS105550

http://identifiers.org/mesh/C566288

http://www.orpha.net/ORDO/Orphanet_275872

id

MONDO:0017161

should conform to

http://purl.obolibrary.org/obo/mondo/patterns/OMIM_phenotypic_series.yaml