Terminology Service for NFDI4Health

hereditary spastic paraplegia 28

Go to external page http://purl.obolibrary.org/obo/DOID_0110779


A hereditary spastic paraplegia that has_material_basis_in mutation in the DDHD1 gene on chromosome 14q22. [ http://purl.obolibrary.org/obo/ECO_0007645 ]

Term info

Label

hereditary spastic paraplegia 28

Synonyms
  • SPG28
  • autosomal recessive spastic paraplegia 28
  • autosomal recessive spastic paraplegia type 28
database cross reference
has obo namespace

disease_ontology

id

DOID:0110779