Disease #00182 (SQT1 (SHORT QT SYNDROME 1), OMIM:609620)

Official abbreviation SQT1
Name SHORT QT SYNDROME 1
OMIM ID 609620
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene KCNH2
Associated tissues -
Disease features -
Remarks -
Date created 2023-06-30 09:44:32 +00:00 (UTC)
Date last edited N/A

  Powered by LOVD v.3.0 Build 30
LOVD software ©2004-2024 Leiden University Medical Center 		There are currently no updates.