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hereditary spastic paraplegia 28
Summary
- Synonym
-
- SPG28
- autosomal recessive spastic paraplegia 28
- autosomal recessive spastic paraplegia type 28
- Definition
- A hereditary spastic paraplegia that has_material_basis_in mutation in the DDHD1 gene on chromosome 14q22.
- Super Class
- autosomal recessive disease hereditary spastic paraplegia
External Links
- Disease Ontology
- DOID:0110779
- Mondo Disease Ontology
- ORDO
- OMIM
Related Genes
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0010830 | Impaired tactile sensation |
| HP:0002064 | Spastic gait |
| HP:0003487 | Babinski sign |
| HP:0002936 | Distal sensory impairment |
| HP:0003621 | Juvenile onset |
| HP:0001258 | Spastic paraplegia |
| HP:0002355 | Difficulty walking |
| HP:0000007 | Autosomal recessive inheritance |
| HP:0003593 | Infantile onset |
| HP:0003677 | Slowly progressive |
