Disease #01027 (DCHE (deafness, congenital heart defects, posterior embryotoxon (DCHE)), OMIM:617992)
| Official abbreviation |
DCHE |
| Name |
deafness, congenital heart defects, posterior embryotoxon (DCHE) |
| OMIM ID |
617992 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
- |
| Individuals reported having this disease |
1 |
| Phenotype entries for this disease |
1 |
| Associated with 1 gene |
JAG1 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
| Date last edited |
2019-06-07 11:51:21 +02:00 (CEST) |
Individuals
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