VAN MALDERGEM SYNDROME 2; VMLDS2 |
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VARIANT ABETA2M AMYLOIDOSIS |
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VAS DEFERENS, CONGENITAL BILATERAL APLASIA OF, X-LINKED; CBAVDX |
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VAS DEFERENS, CONGENITAL BILATERAL APLASIA OF; CBAVD |
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VASCULOPATHY, RETINAL, WITH CEREBRAL LEUKODYSTROPHY; RVCL |
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VATER/VACTERL ASSOCIATION |
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VEIN OF GALEN ANEURYSM |
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VELOCARDIOFACIAL SYNDROME |
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VENOUS MALFORMATIONS, MULTIPLE CUTANEOUS AND MUCOSAL; VMCM |
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VENTRICULAR FIBRILLATION, PAROXYSMAL FAMILIAL, 1; VF1 |
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VENTRICULAR SEPTAL DEFECT 1; VSD1 |
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VENTRICULAR SEPTAL DEFECT 2; VSD2 |
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VENTRICULAR SEPTAL DEFECT 3; VSD3 |
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VENTRICULAR TACHYCARDIA, CATECHOLAMINERGIC POLYMORPHIC, 1, WITH OR WITHOUT ATRIAL DYSFUNCTION AND/OR DILATED CARDIOMYOPATHY; CPVT1 |
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VENTRICULOMEGALY WITH CYSTIC KIDNEY DISEASE; VMCKD |
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VERHEIJ SYNDROME; VRJS |
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VERTEBRAL, CARDIAC, RENAL, AND LIMB DEFECTS SYNDROME 1; VCRL1 |
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VERTICAL TALUS, CONGENITAL; CVT |
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VESICOURETERAL REFLUX 3; VUR3 |
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VESICOURETERAL REFLUX 8; VUR8 |
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