Disease #00525 (Crouzon (Crouzon syndrome), OMIM:123500)
Official abbreviation |
Crouzon |
Name |
Crouzon syndrome |
OMIM ID |
123500 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal dominant |
Individuals reported having this disease |
29 |
Phenotype entries for this disease |
29 |
Associated with 1 gene |
FGFR2 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Individuals
|
|