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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