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DO Term : hereditary spastic paraplegia 9B [DOID:0110825] Disease Ontology
Namespace  disease_ontology Obsolete  false
description  A hereditary spastic paraplegia that has_material_basis_in autosomal recessive homozygous or compound heterozygous mutation in the ALDH18A1 gene on chromosome 10q24.
  • synonyms:
  • SPG9B,
  • OMIM:616586,
  • autosomal recessive spastic paraplegia 9B,
  • autosomal recessive complex spastic paraplegia type 9B,
  • 616586,
  • ORDO:447760,
  • ICD10CM:G11.4
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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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