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Disease Ontology Browser
hereditary spastic paraplegia 36 (DOID:0110787)
Alliance: disease page
Synonyms: autosomal dominant spastic paraplegia 36; autosomal dominant spastic paraplegia type 36; SPG36
Alt IDs: OMIM:613096, ICD10CM:G11.4, ORDO:320365
Definition: A hereditary spastic paraplegia that has_material_basis_in variation in the chromosome region 12q23-q24.

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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MGI 6.12
The Jackson Laboratory