Disease #00769 (FGS4 (FG syndrome, type 4 (FGS4)), OMIM:300422)
Official abbreviation |
FGS4 |
Name |
FG syndrome, type 4 (FGS4) |
OMIM ID |
300422 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
X-linked |
Individuals reported having this disease |
1 |
Phenotype entries for this disease |
- |
Associated with 1 gene |
CASK |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
Date last edited |
2021-01-15 09:18:10 +01:00 (CET) |
Individuals
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