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Spastic Paraplegia, Hereditary

Disease ID: disease_node_8225

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DbxrefGARD:6637, ICD10CM:G11.4, ICD9CM:334.1, MESH:D015419, MIM:PS303350, NCI:C140267, SNOMEDCT_US_2023_03_01:267692008, UMLS_CUI:C0037773
SubclassofDOID_607
Data SourceDOID, MESH
SynonymsFrench settlement disease, Strumpell-Lorrain disease, familial spastic paraplegia, hereditary spastic paraparesis
Mesh IdD015419
Mesh LabelSpastic Paraplegia, Hereditary
Mesh SubclassofD015417
Doid Labelhereditary spastic paraplegia
Doid DescriptionA paraplegia that is characterized by progressive stiffness and contraction (spasticity) in the lower limbs. Xref MGI.
Has SymptomSYMP_0000349, SYMP_0000141
Disease Node Iddisease_node_8225
Doid IdDOID_2476
LabelSpastic Paraplegia, Hereditary