Disease #02650 (FCORD2 (dysplasia, cortical, focal type II (FCORD-2)), OMIM:607341)
| Official abbreviation |
FCORD2 |
| Name |
dysplasia, cortical, focal type II (FCORD-2) |
| OMIM ID |
607341 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
- |
| Individuals reported having this disease |
4 |
| Phenotype entries for this disease |
- |
| Associated with 3 genes |
MTOR, TSC1, TSC2 |
| 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
|