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Hereditary Spastic Paraplegia 8

Disease ID: disease_node_16648

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DbxrefGARD:9591, ICD10CM:G11.4, MIM:603563, ORDO:100989
SubclassofDOID_0050736, DOID_2476
Data SourceDOID
SynonymsSPG8, autosomal dominant spastic paraplegia 8, autosomal dominant spastic paraplegia type 8
Doid Labelhereditary spastic paraplegia 8
Doid DescriptionA hereditary spastic paraplegia that has_material_basis_in mutation in the KIAA0196 gene on chromosome 8q24.
Has Material Basis InGENO_0000147
Disease Node Iddisease_node_16648
Doid IdDOID_0110823
LabelHereditary Spastic Paraplegia 8