Disease #06696 (SPG77 (Spastic paraplegia 77, autosomal recessive), OMIM:617046)
| Official abbreviation |
SPG77 |
| Name |
Spastic paraplegia 77, autosomal recessive |
| OMIM ID |
617046 |
| 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 |
FARS2 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2021-12-10 23:20:41 +01:00 (CET) |
| Date last edited |
N/A |
Individuals
|