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hereditary spastic paraplegia 41

Go to external page http://purl.obolibrary.org/obo/DOID_0110793

A hereditary spastic paraplegia that has_material_basis_in variation in the chromosome region 11p14.1-p11.2. [ http://purl.obolibrary.org/obo/ECO_0007645 ]

Term info

Label

hereditary spastic paraplegia 41

Synonyms
  • SPG41
  • autosomal dominant spastic paraplegia 41
  • autosomal dominant spastic paraplegia type 41
database cross reference
has obo namespace

disease_ontology

id

DOID:0110793