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
|