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DO Term : hereditary spastic paraplegia 90A [DOID:0070459] 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 heterozygous mutation in the SPTSSA gene on chromosome 14q13.1.
  • synonyms:
  • SPG90A,
  • 620416,
  • OMIM:620416,
  • autosomal dominant spastic paraplegia 90A
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Disease

Diseases --> Human genes

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Ontology

Ontology Term --> All ancestors

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Ontology Term --> Direct children

Ontology Term --> Direct parents





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