Phenotype #0000160947

Individual ID 00212465
Associated disease CMH
Phenotype details Familial hypertrophic cardiomyopathy (HCM) is a cardiac disorder characterized by left ventricular hypertrophy (LVH), with predominant involvement of the interventricular septum in the absence of other causes of hypertrophy
Diagnosis/Initial hypertrophic cardiomyopathy
Inheritance Unknown
Diagnosis/Definite CMH-4
Age/Examination -
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Protein -
Owner name Peikuan Cong
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2011-08-15 16:06:17 +02:00 (CEST)
Date last edited N/A

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