Disease #05050 (CFEOM-3A (fibrosis of extraocular muscles, congenital, type 3A (CFEOM-3A)), OMIM:600638)
| Official abbreviation |
CFEOM-3A |
| Name |
fibrosis of extraocular muscles, congenital, type 3A (CFEOM-3A) |
| OMIM ID |
600638 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
- |
| Individuals reported having this disease |
- |
| Phenotype entries for this disease |
- |
| Associated with 1 gene |
TUBB3 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2015-09-23 11:00:40 +02:00 (CEST) |
| Date last edited |
N/A |
|
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