Terminology Service for NFDI4Health

hereditary spastic paraplegia 44

Go to external page http://purl.obolibrary.org/obo/DOID_0110796


A hereditary spastic paraplegia that has_material_basis_in mutation in the GJC2 gene on chromosome 1q42. [ http://purl.obolibrary.org/obo/ECO_0007645 ]

Term info

Label

hereditary spastic paraplegia 44

Synonyms
  • SPG44
  • autosomal recessive spastic paraplegia 44
database cross reference
has obo namespace

disease_ontology

id

DOID:0110796