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DO Term : hereditary spastic paraplegia 32 [DOID:0110783] Disease Ontology
Namespace  disease_ontology Obsolete  false
description  A hereditary spastic paraplegia that has_material_basis_in variation in the chromosome region 14q12-q21.
  • synonyms:
  • OMIM:611252,
  • ICD10CM:G11.4,
  • ORDO:171622,
  • SPG32,
  • 611252,
  • GARD:12749,
  • autosomal recessive spastic paraplegia type 32,
  • autosomal recessive spastic paraplegia 32
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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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