Results 1 -
10
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31
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congenital heart disease
- ... Condition NOTCH1 gene mutations are involved in critical congenital heart disease. Individuals with this condition have one or more ...
- ... Health Condition MedlinePlus Genetics provides information about Critical congenital heart disease More About This Health Condition Increased activity (expression) ...
- ... Health Condition MedlinePlus Genetics provides information about Critical congenital heart disease More About This Health Condition MedlinePlus Genetics provides ...
- ... PubMed Mori AD, Bruneau BG. TBX5 mutations and congenital heart disease: Holt-Oram syndrome revealed. Curr Opin Cardiol. 2004 ...
- ... DC. Nuclear/cytoplasmic transport defects in BBS6 underlie congenital heart disease through perturbation of a chromatin remodeling protein. PLoS ...
- ... Health Condition MedlinePlus Genetics provides information about Critical congenital heart disease More About This Health Condition KIAA1025 MEDIATOR COMPLEX ...
- ... is responsible for a very severe form of heart disease called lethal congenital glycogen storage disease of the heart. People with this mutation are born with extremely ...
- ... the PHOX2B gene have been found to cause congenital central hypoventilation ... resulting in severe constipation, intestinal blockage, and enlargement ...
- ... hair; and a potentially life-threatening form of heart disease called arrhythmogenic right ventricular cardiomyopathy (ARVC).The JUP ... one another effectively. Because affected individuals die before heart disease may become apparent, it is unknown whether a ...
- ... including skeletal muscle weakness and a form of heart disease called dilated cardiomyopathy. More About This Health Condition ... of titin-related muscle disorders be grouped as congenital titinopathy. Often, fetuses with this condition move less ...