Disease #00428 (CMD1I (cardiomyopathy, dilated, type 1I (CMD-1I)), OMIM:604765)
| Official abbreviation |
CMD1I |
| Name |
cardiomyopathy, dilated, type 1I (CMD-1I) |
| OMIM ID |
604765 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal dominant |
| Individuals reported having this disease |
1 |
| Phenotype entries for this disease |
1 |
| Associated with 1 gene |
DES |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2014-06-20 20:37:35 +02:00 (CEST) |
| Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
Individuals
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