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DO Term : amyotrophic lateral sclerosis type 13 [DOID:0060204] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

An amyotrophic lateral sclerosis where a mutation that has_material_basis_in the ATXN2 gene on chromosome 12 contributes to suscepitbility.

synonyms:
ALS13,
amyotrophic lateral sclerosis 13

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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