Disease #00784 (FGS2 (FG syndrome, type 2 (FGS-2)), OMIM:300321)
Official abbreviation |
FGS2 |
Name |
FG syndrome, type 2 (FGS-2) |
OMIM ID |
300321 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
X-linked |
Individuals reported having this disease |
1 |
Phenotype entries for this disease |
1 |
Associated with 1 gene |
FLNA |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Individuals
|
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