Disease #00305 (OFD6 (orofaciodigital syndrome, type VI (OFD-6)), OMIM:277170)
| Official abbreviation |
OFD6 |
| Name |
orofaciodigital syndrome, type VI (OFD-6) |
| OMIM ID |
277170 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal recessive |
| Individuals reported having this disease |
- |
| Phenotype entries for this disease |
- |
| Associated with 1 gene |
C5orf42 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2014-01-19 12:29:11 +01:00 (CET) |
| Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
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