Frontotemporal dementia and/or amyotrophic lateral sclerosis 8

Preferred Label : Frontotemporal dementia and/or amyotrophic lateral sclerosis 8;

Symbol : FTDALS8;

Type : Phenotype, molecular basis known;

Prefixed ID : #619132;

Details

Origin ID

619132;

UMLS CUI

C5436881;

Genes related to phenotype
- Cyld lysine-63 deubiquitinase [OMIM gene]
HPO term(s)
- Amyotrophic lateral sclerosis [HPO term]
- Aphasia [HPO term]
- Autosomal dominant inheritance [HPO term]
- Behavioral abnormality [HPO term]
- Dementia [HPO term]
- Dyscalculia [HPO term]
- Echolalia [HPO term]
- Frontotemporal dementia [HPO term]
- Global brain atrophy [HPO term]
- Impaired executive functioning [HPO term]
- Late onset [HPO term]
- Memory impairment [HPO term]
- Middle age onset [HPO term]
- Neurofibrillary tangles [HPO term]
- Young adult onset [HPO term]
ORDO concept(s)
- Behavioral variant of frontotemporal dementia [ORDO Disease]
See also inter- (CISMeF)
- Behavioral variant of frontotemporal dementia [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]

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