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Hereditary Spastic Paraplegia 51

Disease ID: disease_node_16668

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DbxrefGARD:10999, MIM:613744, ORDO:280763
SubclassofDOID_2476, DOID_0050737
Data SourceDOID
SynonymsCPSQ4, SPG51, autosomal dominant spastic paraplegia 51, spastic quadriplegic cerebral palsy 4
Doid Labelhereditary spastic paraplegia 51
Doid DescriptionA hereditary spastic paraplegia that has_material_basis_in mutation in the AP4E1 gene on chromosome 15q21.
Has Material Basis InGENO_0000148
Disease Node Iddisease_node_16668
Doid IdDOID_0110803
LabelHereditary Spastic Paraplegia 51