Disease #00263 (OFD9 (orofaciodigital syndrome, type 9), OMIM:258865)
| Official abbreviation |
OFD9 |
| Name |
orofaciodigital syndrome, type 9 |
| OMIM ID |
258865 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal recessive |
| Individuals reported having this disease |
2 |
| Phenotype entries for this disease |
2 |
| Associated with 1 gene |
TBC1D32 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2013-10-31 13:51:12 +01:00 (CET) |
| Date last edited |
2026-06-27 17:19:03 +02:00 (CEST) |
Individuals
|