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DO Term : hereditary spastic paraplegia 62 [DOID:0110813] Disease Ontology
Namespace  disease_ontology Obsolete  false
description  A hereditary spastic paraplegia that has_material_basis_in mutation in the ERLIN1 gene on chromosome 10q24.
  • synonyms:
  • OMIM:615681,
  • SPG62,
  • 615681,
  • ICD10CM:G11.4,
  • ORDO:401785,
  • autosomal recessive spastic paraplegia 62,
  • autosomal recessive spastic paraplegia type 62
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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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