Disease #03510 (DKCA-2;DCKB-4 (dyskeratosis congenita, autosomal dominant, type 2 (DKCA-2, autosomal recessive (DKCB-4))), OMIM:613989)
| Official abbreviation |
DKCA-2;DCKB-4 |
| Name |
dyskeratosis congenita, autosomal dominant, type 2 (DKCA-2, autosomal recessive (DKCB-4)) |
| OMIM ID |
613989 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
- |
| Individuals reported having this disease |
- |
| Phenotype entries for this disease |
- |
| Associated with 1 gene |
TERT |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
| Date last edited |
N/A |
|
