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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:0012866 - hereditary spastic paraplegia 35 |
Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee