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Disease Ontology Browser
hereditary spastic paraplegia 43 (DOID:0110795)
Alliance: disease page
Synonyms: autosomal recessive spastic paraplegia 43; autosomal recessive spastic paraplegia type 43; SPG43
Alt IDs: OMIM:615043, ICD10CM:G11.4, ORDO:320370
Definition: A hereditary spastic paraplegia that has_material_basis_in mutation in the C19ORF12 gene on chromosome 19q12.

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB), Gene Ontology (GO)
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last database update
MGI 6.17
The Jackson Laboratory