Terminology Service for NFDI4Health
JSON

hereditary spastic paraplegia 49

Go to external page http://purl.obolibrary.org/obo/DOID_0110801

A hereditary spastic paraplegia that has_material_basis_in mutation in the TECPR2 gene on chromosome 14q32. [ http://purl.obolibrary.org/obo/ECO_0007645 ]

Term info

Label

hereditary spastic paraplegia 49

Synonyms
  • SPG49
  • autosomal recessive spastic paraplegia 49
  • autosomal recessive spastic paraplegia type 49
database cross reference
has obo namespace

disease_ontology

id

DOID:0110801