Disease #00262 (FXS (fragile-X syndrome (FXS)), OMIM:300624)
Official abbreviation |
FXS |
Name |
fragile-X syndrome (FXS) |
OMIM ID |
300624 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
X-linked dominant |
Individuals reported having this disease |
4 |
Phenotype entries for this disease |
2 |
Associated with 1 gene |
FMR1 |
Associated tissues |
- |
Disease features |
- |
Remarks |
X-linked dominant |
Individuals
|
|