Terminology Service for NFDI4Health

hereditary spastic paraplegia 16

Go to external page http://purl.obolibrary.org/obo/DOID_0110769


A hereditary spastic paraplegia that has_material_basis_in variation in the chromosome region Xq11.2. [ http://purl.obolibrary.org/obo/ECO_0007645 ]

Term info

Label

hereditary spastic paraplegia 16

Synonyms
  • SPG16
  • X-linked spastic paraplegia 16
  • X-linked spastic paraplegia type 16
database cross reference
has obo namespace

disease_ontology

id

DOID:0110769