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DOID:0110803 - hereditary spastic paraplegia 51
Disease Ontology Definition:A hereditary spastic paraplegia that has_material_basis_in mutation in the AP4E1 gene on chromosome 15q21.
Synonyms: CPSQ4, SPG51, autosomal dominant spastic paraplegia 51, spastic quadriplegic cerebral palsy 4,
Echinobase Genes : ap4e1
MIM:613744 - spastic paraplegia 51, autosomal recessive; spg51 |
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)