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DO Term : amyotrophic lateral sclerosis type 5 [DOID:0060197] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

An amyotrophic lateral sclerosis that has_material_basis_in mutation in the SPG11 gene on chromosome 15q21.

synonyms:
602099,
amyotrophic lateral sclerosis 5,
ALS5,
GARD:10503,
OMIM:602099

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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