Disease #03509 (DKCB3 (dyskeratosis congenita, autosomal recessive, type 3 (DKCB-3)), OMIM:613988)
| Official abbreviation |
DKCB3 |
| Name |
dyskeratosis congenita, autosomal recessive, type 3 (DKCB-3) |
| OMIM ID |
613988 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal recessive |
| Individuals reported having this disease |
3 |
| Phenotype entries for this disease |
3 |
| Associated with 1 gene |
WRAP53 |
| 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) |
Individuals
|