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DO Term : hereditary spastic paraplegia 57 [DOID:0110809] Disease Ontology
Namespace  disease_ontology Obsolete  false
description  A hereditary spastic paraplegia that has_material_basis_in mutation in the TFG gene on chromosome 3q12.
  • synonyms:
  • autosomal recessive spastic paraplegia type 57,
  • OMIM:615658,
  • autosomal recessive spastic paraplegia 57,
  • ICD10CM:G11.4,
  • ORDO:431329,
  • 615658,
  • SPG57
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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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