Disease #05942 (CHDED (heart defects, congenital and ectodermal dysplasia (CHDED)), OMIM:617364)
| Official abbreviation |
CHDED |
| Name |
heart defects, congenital and ectodermal dysplasia (CHDED) |
| OMIM ID |
617364 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal dominant |
| Individuals reported having this disease |
- |
| Phenotype entries for this disease |
- |
| Associated with 1 gene |
PRKD1 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2021-05-22 20:30:08 +02:00 (CEST) |
| Date last edited |
N/A |
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