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DOID:0110802 - hereditary spastic paraplegia 50
Disease Ontology Definition:A hereditary spastic paraplegia that has_material_basis_in mutation in the AP4M1 gene on chromosome 7q22.1.
Synonyms: CPSQ3, SPG50, autosomal recessive spastic paraplegia 50, spastic quadriplegic cerebral palsy 3,
Echinobase Genes : ap4m1
MIM:612936 - spastic paraplegia 50, autosomal recessive; spg50 |
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)