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DOID:0110808 - hereditary spastic paraplegia 56
Disease Ontology Definition:A hereditary spastic paraplegia that has_material_basis_in mutation in the CYP2U1 gene on chromosome 4q25.
Synonyms: SPG56, autosomal recessive spastic paraplegia 56, autosomal recessive spastic paraplegia type 56,
Echinobase Genes : LOC581885
MIM:615030 - spastic paraplegia 56, autosomal recessive; spg56 |
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
hereditary spastic paraplegia (is_a)