Disease #06939 (HDKR (Hardikar syndrome), OMIM:301068)
| Official abbreviation |
HDKR |
| Name |
Hardikar syndrome |
| OMIM ID |
301068 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
X-linked dominant |
| Individuals reported having this disease |
1 |
| Phenotype entries for this disease |
1 |
| Associated with 1 gene |
MED12 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2022-04-28 20:53:33 +02:00 (CEST) |
| Date last edited |
N/A |
Individuals
|