Disease #00752 (ICF-1 (immunodeficiency-centromeric instability-facial anomalies syndrome, type 1 (ICF-1)), OMIM:242860)
| Official abbreviation |
ICF-1 |
| Name |
immunodeficiency-centromeric instability-facial anomalies syndrome, type 1 (ICF-1) |
| OMIM ID |
242860 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
- |
| Individuals reported having this disease |
- |
| Phenotype entries for this disease |
- |
| Associated with 1 gene |
DNMT3B |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
| Date last edited |
N/A |
|
