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hereditary spastic paraplegia 31
Summary
- Synonym
-
- SPG31
- autosomal dominant spastic paraplegia 31
- autosomal dominant spastic paraplegia type 31
- Definition
- A hereditary spastic paraplegia that has_material_basis_in mutation in the REEP1 gene on chromosome 2p11.
- Super Class
- autosomal dominant disease hereditary spastic paraplegia
External Links
- Disease Ontology
- DOID:0110782
- Mondo Disease Ontology
- ORDO
- OMIM
- GARD
- MGI genotype (from TogoID)
