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Human Disease Vocabulary Browser
The current vocabulary contains human disease, syndrome, and condition terms from Online Mendelian Inheritance in Man (OMIM database).

Browse vocabulary terms by beginning character
 
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Human Diseases/Syndromes Beginning with "V"

To see all annotations for a disease, click the disease name.

OMIM IDHuman Disease
OMIM:276950 Vacterl Association with Hydrocephalus
OMIM:314390 Vacterl Association, X-Linked, with or without Hydrocephalus;
OMIM:601846 Vacuolar Neuromyopathy
OMIM:277100 Valinemia
OMIM:609442 Valproate Embryopathy, Susceptibility to
OMIM:277150 Van Bogaert-Hozay Syndrome
OMIM:607636 Van Buchem Disease, Type 2
OMIM:314500 Van Den Bosch Syndrome
OMIM:600920 Van Den Ende-Gupta Syndrome; VDEGS
OMIM:119300 Van Der Woude Syndrome 1; VWS1
OMIM:606713 Van Der Woude Syndrome 2; VWS2
OMIM:603570 Vanin 1; VNN1
OMIM:601390 Van Maldergem Syndrome 1; VMLDS1
OMIM:615546 Van Maldergem Syndrome 2; VMLDS2
OMIM:600670 Varicella, Severe Recurrent
OMIM:192200 Varicose Veins
OMIM:192240 Vascular Endothelial Growth Factor A; VEGFA
OMIM:192300 Vascular Helix of Umbilical Cord
OMIM:277175 Vascular Hyalinosis
OMIM:606893 Vascular Malformation, Primary Intraosseous
OMIM:609817 Vasculitis, Lymphocytic, Cutaneous Small Vessel
OMIM:192310 Vasculitis, Lymphocytic, Nodular
OMIM:192315 Vasculopathy, Retinal, with Cerebral Leukodystrophy; RVCL
OMIM:277180 Vas Deferens, Congenital Bilateral Aplasia Of; CBAVD
OMIM:300985 Vas Deferens, Congenital Bilateral Aplasia of, X-Linked; CBAVDX
OMIM:608406 Vater-Like Defects with Pulmonary Hypertension, Laryngeal Webs, and Growth Deficiency
OMIM:192350 Vater/Vacterl Association
OMIM:192400 Veins, Pattern of, on Anterior Thorax
OMIM:192430 Velocardiofacial Syndrome
OMIM:600736 Velofacioskeletal Syndrome
OMIM:600195 Venous Malformations, Multiple Cutaneous and Mucosal; VMCM
OMIM:192445 Ventricular Extrasystoles with Syncope, Perodactyly, and Robin Sequence
OMIM:603829 Ventricular Fibrillation, Paroxysmal Familial, 1; VF1
OMIM:612956 Ventricular Fibrillation, Paroxysmal Familial, 2; VF2
OMIM:614429 Ventricular Septal Defect 1; VSD1
OMIM:614431 Ventricular Septal Defect 2; VSD2
OMIM:614432 Ventricular Septal Defect 3; VSD3
OMIM:604772 Ventricular Tachycardia, Catecholaminergic Polymorphic, 1, with or without Atrial Dysfunction and/or Dilated Cardiomyopathy; CPVT1
OMIM:611938 Ventricular Tachycardia, Catecholaminergic Polymorphic, 2; CPVT2
OMIM:614021 Ventricular Tachycardia, Catecholaminergic Polymorphic, 3; CPVT3
OMIM:614916 Ventricular Tachycardia, Catecholaminergic Polymorphic, 4; CPVT4
OMIM:615441 Ventricular Tachycardia, Catecholaminergic Polymorphic, 5, with or without Muscle Weakness; CPVT5
OMIM:192605 Ventricular Tachycardia, Familial
OMIM:219730 Ventriculomegaly with Cystic Kidney Disease; VMCKD
OMIM:602200 Ventriculomegaly with Defects of the Radius and Kidney
OMIM:192700 Venular Insufficiency, Systemic
OMIM:615583 Verheij Syndrome; VRJS
OMIM:617660 Vertebral, Cardiac, Renal, and Limb Defects Syndrome 1; VCRL1
OMIM:617661 Vertebral, Cardiac, Renal, and Limb Defects Syndrome 2; VCRL2
OMIM:192800 Vertebral Fusion, Posterior Lumbosacral, with Blepharoptosis
OMIM:192900 Vertebral Hypoplasia with Lumbar Kyphosis
OMIM:192950 Vertical Talus, Congenital; CVT
OMIM:613106 Vertigo, Benign Recurrent, 2; BRV2
OMIM:193007 Vertigo, Benign Recurrent; BRV
OMIM:193000 Vesicoureteral Reflux 1; VUR1
OMIM:610878 Vesicoureteral Reflux 2; VUR2
OMIM:613674 Vesicoureteral Reflux 3; VUR3
OMIM:614317 Vesicoureteral Reflux 4; VUR4
OMIM:614318 Vesicoureteral Reflux 5; VUR5
OMIM:614319 Vesicoureteral Reflux 6; VUR6
OMIM:615390 Vesicoureteral Reflux 7; VUR7
OMIM:615963 Vesicoureteral Reflux 8; VUR8
OMIM:314550 Vesicoureteral Reflux, X-Linked; VURX
OMIM:193005 Vestibulocochlear Dysfunction, Progressive
OMIM:125630 Vibratory Urticaria; VBU
OMIM:242840 Vici Syndrome; VICIS
OMIM:193070 Virus Rd114 RNA Complementarity
OMIM:277320 Visceral Myopathy, Familial, with External Ophthalmoplegia
OMIM:155310 Visceral Myopathy; VSCM
OMIM:609629 Visceral Neuropathy, Familial, Autosomal Dominant
OMIM:243180 Visceral Neuropathy, Familial, Autosomal Recessive
OMIM:228100 Visceral Steatosis, Congenital
OMIM:277440 Vitamin D-Dependent Rickets, Type 2A; VDDR2A
OMIM:600785 Vitamin D-Dependent Rickets, Type 2b, with Normal Vitamin D Receptor;
OMIM:264700 Vitamin D Hydroxylation-Deficient Rickets, Type 1A; VDDR1A
OMIM:600081 Vitamin D Hydroxylation-Deficient Rickets, Type 1B; VDDR1B
OMIM:277460 Vitamin E, Familial Isolated Deficiency Of; VED
OMIM:277450 Vitamin K-Dependent Clotting Factors, Combined Deficiency of, 1; VKCFD1
OMIM:607473 Vitamin K-Dependent Clotting Factors, Combined Deficiency of, 2; VKCFD2
OMIM:606579 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1;
OMIM:193200 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6;
OMIM:277465 Vitiligo, Progressive, with Mental Retardation and Urethral Duplication
OMIM:193230 Vitreoretinal Degeneration, Snowflake Type; SVD
OMIM:193220 Vitreoretinochoroidopathy; VRCP
OMIM:193235 Vitreoretinopathy, Neovascular Inflammatory; VRNI
OMIM:193240 Vocal Cord Paralysis and Ptosis
OMIM:604117 Vohwinkel Syndrome, Variant Form
OMIM:124500 Vohwinkel Syndrome; VOWNKL
OMIM:193250 Volvulus of Midgut
OMIM:193300 Von Hippel-Lindau Syndrome; VHL
OMIM:193400 Von Willebrand Disease, Type 1; VWD1
OMIM:613554 Von Willebrand Disease, Type 2; VWD2
OMIM:277480 Von Willebrand Disease, Type 3; VWD3
OMIM:314560 Von Willebrand Disease, X-Linked Form
OMIM:193450 Vulvovaginitis, Allergic Seminal

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last database update
11/07/2017
MGI 6.11
The Jackson Laboratory