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DO Term : frontotemporal dementia and/or amyotrophic lateral sclerosis 2 [DOID:0060214] Disease Ontology
Namespace  disease_ontology Obsolete  false
description  An amyotrophic lateral sclerosis that has_material_basis_in mutation in the CHCHD10 gene on chromosome 22. It is characterized by adult onset of either frontotemporal dementia and/or amyotrophic lateral sclerosis.
  • synonyms:
  • OMIM:615911,
  • FTDALS2,
  • 615911
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Disease

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Ontology

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Ontology Term --> Direct parents





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