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DO Term : amyotrophic lateral sclerosis type 1 [DOID:0060193] Disease Ontology
Namespace  disease_ontology Obsolete  false
description  An amyotrophic lateral sclerosis that has_material_basis_in mutation in the SOD1 gene on chromosome 21. The most common type of familial ALS.
  • synonyms:
  • ALS1,
  • OMIM:105400,
  • ICD10CM:G12.2,
  • amyotrophic lateral sclerosis 1,
  • 105400
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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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