Disease #06952 (DELMNES (Delpire-McNeill syndrome), OMIM:619083)
| Official abbreviation |
DELMNES |
| Name |
Delpire-McNeill syndrome |
| OMIM ID |
619083 |
| 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 |
SLC12A2 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2022-08-05 13:51:14 +02:00 (CEST) |
| Date last edited |
N/A |
Individuals
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