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hereditary spastic paraplegia 43

Go to external page http://purl.obolibrary.org/obo/DOID_0110795

A hereditary spastic paraplegia that has_material_basis_in mutation in the C19ORF12 gene on chromosome 19q12. [ http://purl.obolibrary.org/obo/ECO_0007645 ]

Term info

Label

hereditary spastic paraplegia 43

Synonyms
  • SPG43
  • autosomal recessive spastic paraplegia 43
  • autosomal recessive spastic paraplegia type 43
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disease_ontology

id

DOID:0110795