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hereditary spastic paraplegia 63

Go to external page http://purl.obolibrary.org/obo/DOID_0110814

A hereditary spastic paraplegia that has_material_basis_in mutation in the AMPD2 gene on chromosome 1p13. [ http://purl.obolibrary.org/obo/ECO_0007645 ]

Term info

Label

hereditary spastic paraplegia 63

Synonyms
  • SPG63
  • autosomal recessive spastic paraplegia 63
  • spastic paraplegia 63
database cross reference
has obo namespace

disease_ontology

id

DOID:0110814