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DOID:0110768 - hereditary spastic paraplegia 15
Disease Ontology Definition:A hereditary spastic paraplegia that has_material_basis_in mutation in the ZFYVE26 gene on chromosome 14q24.1.
Synonyms: Kjellin syndrome, SPG15, autosomal recessive spastic paraplegia 15, autosomal recessive spastic paraplegia type 15, hereditary spastic paraparesis type 15, spastic paraplegia and retinal degeneration, spastic paraplegia-retinal degeneration syndrome,
Echinobase Genes :
MIM:270700 - spastic paraplegia 15, autosomal recessive; spg15 |
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)