Disease #00867 (OFC6 (orofacial cleft, type 6 (OFC-6)), OMIM:608864)
| Official abbreviation |
OFC6 |
| Name |
orofacial cleft, type 6 (OFC-6) |
| OMIM ID |
608864 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal dominant |
| Individuals reported having this disease |
- |
| Phenotype entries for this disease |
- |
| Associated with 1 gene |
IRF6 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
| Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
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