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Human Disease
hereditary spastic paraplegia 53
- Term ID
- DOID:0110805
- Synonyms
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- autosomal recessive spastic paraplegia 53
- autosomal recessive spastic paraplegia type 53
- SPG53
- Definition
- A hereditary spastic paraplegia that has_material_basis_in mutation in the VPS37A gene on chromosome 8p22. https://www.ncbi.nlm.nih.gov/pubmed/22717650
- References
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- ICD10CM:G11.4
- MIM:614898
- ORDO:319199
- Ontology
- Human Disease ( DOID:0110805 )
- is a type of
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