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Hereditary Spastic Paraplegia 16

Disease ID: disease_node_16639

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DbxrefGARD:9585, ICD10CM:G11.4, MIM:300266, ORDO:100997
SubclassofDOID_0080012, DOID_2476
Data SourceDOID
SynonymsSPG16, X-linked spastic paraplegia 16, X-linked spastic paraplegia type 16
Doid Labelhereditary spastic paraplegia 16
Doid DescriptionA hereditary spastic paraplegia that has_material_basis_in variation in the chromosome region Xq11.2.
Has Material Basis InGENO_0000149
Disease Node Iddisease_node_16639
Doid IdDOID_0110769
LabelHereditary Spastic Paraplegia 16