Disease #04239 (hypometh. (hypomethylation))
| Official abbreviation |
hypometh. |
| Name |
hypomethylation |
| OMIM ID |
- |
| Inheritance |
Autosomal dominant, Autosomal recessive |
| Individuals reported having this disease |
1 |
| Phenotype entries for this disease |
1 |
| Associated with 0 genes |
- |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2015-04-06 21:46:14 +02:00 (CEST) |
| Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
Individuals
|