Cardiac Valvular Defect, Developmental; Cvdd
Clinical Features
Top most frequent phenotypes and symptoms related to Cardiac Valvular Defect, Developmental; Cvdd
- Ventricular septal defect
- Edema
- Atrial septal defect
- Hernia
- Inguinal hernia
- Hydronephrosis
- Abnormal cardiac septum morphology
- Pulmonic stenosis
- Cyanosis
- Mitral valve prolapse
And another 12 symptoms. If you need more information about this disease we can help you.
Incidence and onset information
— Currently we don't have prevalence information about this disease (Not enough data available about incidence and published cases.)— No data available about the known clinical features onset.
Researches and researchers
Currently, we don't have any information about doctors, researches or researchers related to this disease. Please contact us if you would like to appear here.Cardiac Valvular Defect, Developmental; Cvdd Recommended genes panels
| Panel Name, Specifity and genes Tested/covered |
|---|
 PLD1.
By Fulgent Genetics Fulgent Genetics (United States).
PLD1
Specificity
100 %
Genes
100 % |
You can get up to -7 more panels with our dedicated tool
Learn moreSources and references
You can check the following sources for additional information.
OMIM MESH Rare Disease Symptoms CheckerIf you liked this article maybe you will also find interesting the following in-depth articles about other rare diseases, like MYOPATHY, TUBULAR AGGREGATE, 1; TAM1 OBESITY DUE TO MELANOCORTIN 4 RECEPTOR DEFICIENCY EPILEPSY, MYOCLONIC JUVENILE; EJM GLYCOGEN STORAGE DISEASE DUE TO LIVER GLYCOGEN PHOSPHORYLASE DEFICIENCY ACYL-CoA DEHYDROGENASE, SHORT-CHAIN, DEFICIENCY OF; ACADSD VENTRICULAR TACHYCARDIA, CATECHOLAMINERGIC POLYMORPHIC, 1, WITH OR WITHOUT ATRIAL DYSFUNCTION AND/OR DILATED CARDIOMYOPATHY; CPVT1 NEPHROTIC SYNDROME, TYPE 1; NPHS1