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DOID:0110813 - hereditary spastic paraplegia 62
Disease Ontology Definition:A hereditary spastic paraplegia that has_material_basis_in mutation in the ERLIN1 gene on chromosome 10q24.
Synonyms: SPG62, autosomal recessive spastic paraplegia 62, autosomal recessive spastic paraplegia type 62,
Xenbase Genes
![Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries](img/icons/info1.png)
MONDO:0014302 - hereditary spastic paraplegia 62 |
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee