Amyotrophic lateral sclerosis 26 with or without frontotemporal dementia

Preferred Label : Amyotrophic lateral sclerosis 26 with or without frontotemporal dementia;

Symbol : ALS26;

Type : Phenotype, molecular basis known;

Prefixed ID : #619133;

Details

Origin ID

619133;

UMLS CUI

C5436882;

Genes related to phenotype
- Tia1 cytotoxic granule-associated rna-binding protein [OMIM gene]
HPO term(s)
- Amyotrophic lateral sclerosis [HPO term]
- Aphasia [HPO term]
- Autosomal dominant inheritance [HPO term]
- Bulbar palsy [HPO term]
- Frontotemporal dementia [HPO term]
- Late onset [HPO term]
- Lewy bodies [HPO term]
- Limb muscle weakness [HPO term]
- Memory impairment [HPO term]
- Middle age onset [HPO term]
- Personality changes [HPO term]
- Young adult onset [HPO term]
ORDO concept(s)
- Amyotrophic lateral sclerosis [ORDO Disease]
- Frontotemporal dementia with motor neuron disease [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]

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