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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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VISCERAL MYOPATHY; VSCM |
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VITAMIN B12-UNRESPONSIVE METHYLMALONIC ACIDEMIA TYPE MUT- |
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VITAMIN B12-UNRESPONSIVE METHYLMALONIC ACIDEMIA TYPE MUT0 |
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VITAMIN D HYDROXYLATION-DEFICIENT RICKETS, TYPE 1A; VDDR1A |
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VITAMIN D HYDROXYLATION-DEFICIENT RICKETS, TYPE 1B; VDDR1B |
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VITAMIN D-DEPENDENT RICKETS, TYPE 2A; VDDR2A |
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VITAMIN K-DEPENDENT CLOTTING FACTORS, COMBINED DEFICIENCY OF, 1; VKCFD1 |
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VITILIGO-ASSOCIATED MULTIPLE AUTOIMMUNE DISEASE SUSCEPTIBILITY 1; VAMAS1 |
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