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DOID:0110801 - hereditary spastic paraplegia 49
Disease Ontology Definition:A hereditary spastic paraplegia that has_material_basis_in mutation in the TECPR2 gene on chromosome 14q32.
Synonyms: SPG49, autosomal recessive spastic paraplegia 49, autosomal recessive spastic paraplegia type 49,
Echinobase Genes : tecpr2
MIM:615031 - spastic paraplegia 49, autosomal recessive; spg49 |
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)