Search Ontology:
Human Disease
hereditary spastic paraplegia 29
- Term ID
- DOID:0110780
- Synonyms
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- autosomal dominant spastic paraplegia 29
- SPG29
- Definition
- A hereditary spastic paraplegia that has_material_basis_in variation in the chromosome region 1p31.1-p21.1. https://www.ncbi.nlm.nih.gov/pubmed/16130112
- References
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- GARD:9729
- ICD10CM:G11.4
- MIM:609727
- ORDO:101009
- Ontology
- Human Disease ( DOID:0110780 )
- is a type of
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Zebrafish Models