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Human Disease
hereditary spastic paraplegia 54
- Term ID
- DOID:0110806
- Synonyms
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- autosomal recessive spastic paraplegia 54
- autosomal recessive spastic paraplegia type 54
- SPG54
- Definition
- A hereditary spastic paraplegia that has_material_basis_in mutation in the DDHD2 gene on chromosome 8p11. https://www.ncbi.nlm.nih.gov/pubmed/23176823
- References
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- ICD10CM:G11.4
- MIM:615033
- ORDO:320380
- Ontology
- Human Disease ( DOID:0110806 )
- is a type of
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