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DO Term : amyotrophic lateral sclerosis type 2 [DOID:0060194] Disease Ontology
Namespace  disease_ontology Obsolete  false
description  An amyotrophic lateral sclerosis that has_material_basis_in mutation in the alsin gene on chromosome 2.
  • synonyms:
  • amyotrophic lateral sclerosis 2, juvenile,
  • GARD:9470,
  • amyotrophic lateral sclerosis 2,
  • ALS2,
  • ICD10CM:G12.2,
  • 205100,
  • OMIM:205100
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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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