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DO Term : amyotrophic lateral sclerosis type 6 [DOID:0060198] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

An amyotrophic lateral sclerosis that has_material_basis_in mutation in the FUS gene on chromosome 16.

synonyms:
608030,
OMIM:608030,
ALS6,
GARD:9874,
autosomal recessive amyotrophic lateral sclerosis 6,
amyotrophic lateral sclerosis 6, 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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