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Summary Literature (0)
DOID:0110786 - hereditary spastic paraplegia 35

Disease Ontology Definition:A hereditary spastic paraplegia that has_material_basis_in mutation in the FA2H gene on chromosome 16q23.1.

Synonyms: FAHN, 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

Xenbase Genes : fa2h

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0012866 - hereditary spastic paraplegia 35

Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): hereditary spastic paraplegia (is_a)