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Hereditary Spastic Paraplegia 35

Disease ID: disease_node_16693

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DbxrefICD10CM:G11.4, MIM:612319, ORDO:171629
SubclassofDOID_2476, DOID_0050737
Data SourceDOID
SynonymsFAHN, SPG35, autosomal recessive spastic paraplegia 35, autosomal recessive spastic paraplegia type 35, fatty acid hydroxylase-associated neurodegeneration, leukodystrophy, dysmyelinating and spastic paraparesis with or without dystonia
Doid Labelhereditary spastic paraplegia 35
Doid DescriptionA hereditary spastic paraplegia that has_material_basis_in mutation in the FA2H gene on chromosome 16q23.1.
Has Material Basis InGENO_0000148
Disease Node Iddisease_node_16693
Doid IdDOID_0110786
LabelHereditary Spastic Paraplegia 35