Frontotemporal Dementia and/or Amyotrophic Lateral Sclerosis 2

Preferred Label : Frontotemporal Dementia and/or Amyotrophic Lateral Sclerosis 2;

NCIt synonyms : FTDALS2;

NCIt definition : An autosomal dominant form of frontotemporal dementia and/or amyotrophic lateral sclerosis caused by mutation(s) in the CHCHD10 gene, encoding coiled-coil-helix-coiled-coil-helix domain-containing protein 10, mitochondrial.;

Détails

Origin ID

C214862;

Has associated anatomic sites
- Central Nervous System [NCIt concept]
- Nervous System [NCIt concept]
concept_is_in_subset
- Cellosaurus Disease Terminology [NCIt concept]
disease_has_primary_anatomic_site
- Central Nervous System [NCIt concept]
- Nervous System [NCIt concept]
disease_mapped_to_gene
- CHCHD10 Gene [NCIt concept]

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