Disease #00047
Official abbreviation |
COFS2 |
Name |
Cerebrooculofacioskeletal syndrome 2 |
OMIM ID |
610756 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
- |
Individuals reported having this disease |
0 |
Phenotype entries for this disease |
0 |
Associated with 1 gene |
ERCC2 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
|
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