Disease #00214 (SPG12 (paraplegia, spastic, autosomal dominant, type 12 (SPG-12)), OMIM:604805)
| Official abbreviation |
SPG12 |
| Name |
paraplegia, spastic, autosomal dominant, type 12 (SPG-12) |
| OMIM ID |
604805 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal dominant |
| Individuals reported having this disease |
1 |
| Phenotype entries for this disease |
1 |
| Associated with 1 gene |
RTN2 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2013-10-02 11:35:03 +02:00 (CEST) |
| Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
Individuals
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