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DO Term : hereditary spastic paraplegia 90B [DOID:0070460] Disease Ontology
Namespace  disease_ontology Obsolete  false
description  A hereditary spastic paraplegia characterized by motor impairment and progressive lower limb spasticity that has_material_basis_in homozygous mutation in the SPTSSA gene on chromosome 14q13.1.
  • synonyms:
  • OMIM:620417,
  • SPG90B,
  • autosomal recessive spastic paraplegia 90B,
  • 620417
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Disease

Diseases --> Human genes

Diseases --> Mouse genes

Diseases --> Mouse models

Ontology

Ontology Term --> All ancestors

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Ontology Term --> Direct children

Ontology Term --> Direct parents





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