Disease #00158 (SHORT QT SYNDROME (SHORT QT SYNDROME 2), OMIM:609621)
Official abbreviation |
SHORT QT SYNDROME |
Name |
SHORT QT SYNDROME 2 |
OMIM ID |
609621 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal dominant |
Individuals reported having this disease |
- |
Phenotype entries for this disease |
- |
Associated with 1 gene |
KCNQ1 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Date created |
2023-06-27 10:49:29 +00:00 (UTC) |
Date last edited |
N/A |
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