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hereditary spastic paraplegia 37

Go to external page http://purl.obolibrary.org/obo/DOID_0110788

A hereditary spastic paraplegia that has_material_basis_in variation in the chromosome region 8p21.1-q13.3. [ http://purl.obolibrary.org/obo/ECO_0007645 ]

Term info

Label

hereditary spastic paraplegia 37

Synonyms
  • SPG37
  • autosomal dominant spastic paraplegia 37
  • autosomal dominant spastic paraplegia type 37
database cross reference
has obo namespace

disease_ontology

id

DOID:0110788