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DO Term : frontotemporal dementia and/or amyotrophic lateral sclerosis 1 [DOID:0060213] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

An amyotrophic lateral sclerosis that has_material_basis_in mutation in the C9ORF72 gene on chromosome 9. It is characterized by adult onset of either frontotemporal dementia and/or amyotrophic lateral sclerosis.

synonyms:
FTDALS1,
105550,
OMIM:105550,
ALSFTD,
FTDMND,
frontotemporal dementia and/or motor neuron disease,
amyotrophic lateral sclerosis and/or frontotemporal dementia

Disease

Diseases --> Human genes

Diseases --> Mouse genes

Diseases --> Mouse models

Ontology

Ontology Term --> All ancestors

Ontology Term --> All descendants

Ontology Term --> Direct children

Ontology Term --> Direct parents

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