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DO Term : amyotrophic lateral sclerosis type 15 [DOID:0060206] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

An amyotrophic lateral sclerosis that has_material_basis_in mutation in the UBQLN2 gene on chromosome X.

synonyms:
ALS15,
amyotrophic lateral sclerosis 15,
300857,
OMIM:300857,
amyotrophic lateral sclerosis 15, with or without 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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