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hereditary spastic paraplegia 56
Summary
- Synonym
-
- SPG56
- autosomal recessive spastic paraplegia 56
- autosomal recessive spastic paraplegia type 56
- Definition
- A hereditary spastic paraplegia that has_material_basis_in mutation in the CYP2U1 gene on chromosome 4q25.
- Super Class
- autosomal recessive disease hereditary spastic paraplegia
External Links
- Disease Ontology
- DOID:0110808
- Mondo Disease Ontology
- ORDO
- OMIM
Related Genes
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0003577 | Congenital onset |
