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Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
hereditary spastic paraplegia
Summary
- Synonym
-
- French settlement disease
- Strumpell-Lorrain disease
- familial spastic paraplegia
- hereditary spastic paraparesis
- Definition
- A paraplegia that is characterized by progressive stiffness and contraction (spasticity) in the lower limbs.
- Super Class
- paraplegia
External Links
- Disease Ontology
- DOID:2476
- Mondo Disease Ontology
- MeSH
- UMLS
- NCI Thesaurus
- OMIM
- GARD
- MGI genotype (from TogoID)
Related Genes
| Gene ID | Gene Symbol | Description | Source |
|---|---|---|---|
| 823 | CAPN1 | calpain 1 | |
| 825 | CAPN3 | calpain 3 | |
| 1759 | DNM1 | dynamin 1 | |
| 1785 | DNM2 | dynamin 2 | |
| 3329 | HSPD1 | heat shock protein family D (Hsp60) member 1 | |
| 3799 | KIF5B | kinesin family member 5B | |
| 5704 | PSMC4 | proteasome 26S subunit, ATPase 4 | |
| 5832 | ALDH18A1 | aldehyde dehydrogenase 18 family member A1 | |
| 6252 | RTN1 | reticulon 1 | |
| 6253 | RTN2 | reticulon 2 |
| Gene ID | Gene Symbol | Description | Source |
|---|---|---|---|
| 70701 | Nipal1 | NIPA-like domain containing 1 | |
| 74772 | Atp13a2 | ATPase type 13A2 | |
| 103967 | Dnm3 | dynamin 3 | |
| 104001 | Rtn1 | reticulon 1 | |
| 109168 | Atl3 | atlastin GTPase 3 | |
| 214112 | Nipal4 | NIPA-like domain containing 4 | |
| 224088 | Atp13a3 | ATPase type 13A3 | |
| 226144 | Erlin1 | ER lipid raft associated 1 | |
| 244373 | Erlin2 | ER lipid raft associated 2 | |
| 268878 | Atp13a5 | ATPase type 13A5 |
