Disease #01560 (SPG4 (paraplegia, spastic, autosomal dominant, type 4 (SPG4)), OMIM:182601)
| Official abbreviation |
SPG4 |
| Name |
paraplegia, spastic, autosomal dominant, type 4 (SPG4) |
| OMIM ID |
182601 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal dominant |
| Individuals reported having this disease |
12 |
| Phenotype entries for this disease |
12 |
| Associated with 1 gene |
SPAST |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
| Date last edited |
2021-10-07 08:59:33 +02:00 (CEST) |
Individuals
|