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
|