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About: hereditary spastic paraplegia 2     Goto   Sponge   NotDistinct   Permalink

An Entity of Type : owl:Class, within Data Space : linkeddata.uriburner.com:28898 associated with source document(s)

AttributesValues
type
subClassOf
label
  • hereditary spastic paraplegia 2
described by
id
  • DOID:0110773
database_cross_reference
  • GARD:4923
  • ICD10CM:G11.4
  • OMIM:312920
  • ORDO:99015
has_exact_synonym
  • SPG2 (en)
  • X-linked spastic paraplegia 2 (en)
  • spastic paraplegia type 2 (en)
has_obo_namespace
  • disease_ontology
http://purl.obolib...g/obo/IAO_0000115
  • A hereditary spastic paraplegia that has_material_basis_in mutation in the PLP1 gene on chromosome Xq22.2.
is topic of
is annotatedSource of
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