Disease #03784 (SPG53 (paraplegia, spastic, type 53, autosomal recessive (SPG-53)), OMIM:614898)
| Official abbreviation |
SPG53 |
| Name |
paraplegia, spastic, type 53, autosomal recessive (SPG-53) |
| OMIM ID |
614898 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal recessive |
| Individuals reported having this disease |
1 |
| Phenotype entries for this disease |
1 |
| Associated with 1 gene |
VPS37A |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
| Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
Individuals
|