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DO Term : hereditary spastic paraplegia 42 [DOID:0110794] Disease Ontology
Namespace  disease_ontology Obsolete  false
description  A hereditary spastic paraplegia that has_material_basis_in mutation in the SLC33A1 gene on chromosome 3q25.31.
  • synonyms:
  • ICD10CM:G11.4,
  • ORDO:171863,
  • SPG42,
  • 612539,
  • OMIM:612539,
  • autosomal dominant spastic paraplegia 42,
  • autosomal dominant spastic paraplegia type 42
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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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