Spastic paraplegia
Information
- Disease name
- Spastic paraplegia
- Disease ID
- Description
Disease area statistics
Chromosome band
| Gene symbol | Chromosome | Start | Stop | The number of variant |
|---|---|---|---|---|
| L1CAM | X | 153,861,516 | 153,886,173 | 4 |
Annotation
| Genes | Mutation | Description | Source | Links |
|---|
| NCT ID | Status | Phase | Summary | Start date | Completion date |
|---|---|---|---|---|---|
| NCT04006418 | Recruiting | A Registered Cohort Study on Spastic Paraplegia | July 1, 2019 | December 2049 | |
| NCT05432999 | Recruiting | N/A | Extracorporeal Shockwave Therapy for Spasticity in People With Spinal Cord Injury | September 1, 2022 | February 1, 2025 |
| NCT05518188 | Recruiting | Phase 1/Phase 2 | Melpida: Recombinant Adeno-associated Virus (Serotype 9) Encoding a Codon Optimized Human AP4M1 Transgene (hAP4M1opt) | February 15, 2023 | October 1, 2030 |
| NCT05848271 | Recruiting | Natural History Study of Patients With HPDL Mutations | May 1, 2023 | December 31, 2024 | |
| NCT06156813 | Recruiting | Turkish Lower-Extremity Motor Activity Log (LE-MAL) | November 15, 2023 | June 15, 2024 | |
| NCT06260982 | Recruiting | Cognitive Disorders in Hereditary Spastic Paraplegia Type 4 | January 1, 2022 | January 2, 2025 |
- HPO alt_id (Human Phenotype Ontology)
- HP:0007062
- HPO alt_id (Human Phenotype Ontology)
- HP:0007124
- HPO alt_id (Human Phenotype Ontology)
- HP:0007216
- HPO Human Phenotype ID (Human Phenotype Ontology)
- HP:0001258
- OMIM Phenotype Series Number (OMIM)
- PS303350
- ICD10 preferred id (Insert disease from ICD10)
- D0005552
- ICD10 class code (Insert disease from ICD10)
- G82.1