Disease #02650 (FCORD-2 (dysplasia, cortical, focal type II (FCORD-2)), OMIM:607341)
Official abbreviation |
FCORD-2 |
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 |
0 |
Associated with 3 genes |
MTOR, TSC1, TSC2 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Individuals
|
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