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DO Term : hereditary spastic paraplegia 89 [DOID:0070458] Disease Ontology
Namespace  disease_ontology Obsolete  false
description  A hereditary spastic paraplegia characterized by infantile or early childhood onset of lower limb spasticity that has_material_basis_in homozygous mutation in the AMFR gene on chromosome 16q13.
  • synonyms:
  • autosomal recessive spastic paraplegia 89,
  • SPG89,
  • 620379,
  • OMIM:620379
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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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