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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
276950 Vacterl Association with Hydrocephalus (1 mouse models)
314390 Vacterl Association, X-Linked, with or without Hydrocephalus;
601846 Vacuolar Neuromyopathy
277100 Valinemia
609442 Valproate Embryopathy, Susceptibility to
277150 Van Bogaert-Hozay Syndrome
607636 Van Buchem Disease, Type 2
314500 Van Den Bosch Syndrome
600920 Van Den Ende-Gupta Syndrome; VDEGS
119300 Van Der Woude Syndrome 1; VWS1 (1 mouse models)
606713 Van Der Woude Syndrome 2; VWS2 (1 mouse models)
603570 Vanin 1; VNN1
601390 Van Maldergem Syndrome 1; VMLDS1
615546 Van Maldergem Syndrome 2; VMLDS2
600670 Varicella, Severe Recurrent
192200 Varicose Veins
192240 Vascular Endothelial Growth Factor A; VEGFA
192300 Vascular Helix of Umbilical Cord
277175 Vascular Hyalinosis
606893 Vascular Malformation, Primary Intraosseous
609817 Vasculitis, Lymphocytic, Cutaneous Small Vessel
192310 Vasculitis, Lymphocytic, Nodular
192315 Vasculopathy, Retinal, with Cerebral Leukodystrophy; RVCL
277180 Vas Deferens, Congenital Bilateral Aplasia Of; CBAVD
300985 Vas Deferens, Congenital Bilateral Aplasia of, X-Linked; CBAVDX
608406 Vater-Like Defects with Pulmonary Hypertension, Laryngeal Webs, and Growth Deficiency
192350 Vater/Vacterl Association (4 mouse models)
192400 Veins, Pattern of, on Anterior Thorax
192430 Velocardiofacial Syndrome (12 mouse models)
600736 Velofacioskeletal Syndrome
600195 Venous Malformations, Multiple Cutaneous and Mucosal; VMCM
192445 Ventricular Extrasystoles with Syncope, Perodactyly, and Robin Sequence
603829 Ventricular Fibrillation, Paroxysmal Familial, 1; VF1
612956 Ventricular Fibrillation, Paroxysmal Familial, 2; VF2
614429 Ventricular Septal Defect 1; VSD1
614431 Ventricular Septal Defect 2; VSD2
614432 Ventricular Septal Defect 3; VSD3
604772 Ventricular Tachycardia, Catecholaminergic Polymorphic, 1, with or without Atrial Dysfunction and/or Dilated Cardiomyopathy; CPVT1 (8 mouse models)
611938 Ventricular Tachycardia, Catecholaminergic Polymorphic, 2; CPVT2 (4 mouse models)
614021 Ventricular Tachycardia, Catecholaminergic Polymorphic, 3; CPVT3
614916 Ventricular Tachycardia, Catecholaminergic Polymorphic, 4; CPVT4
615441 Ventricular Tachycardia, Catecholaminergic Polymorphic, 5, with or without Muscle Weakness; CPVT5
192605 Ventricular Tachycardia, Familial
219730 Ventriculomegaly with Cystic Kidney Disease; VMCKD
602200 Ventriculomegaly with Defects of the Radius and Kidney
192700 Venular Insufficiency, Systemic
615583 Verheij Syndrome; VRJS
192800 Vertebral Fusion, Posterior Lumbosacral, with Blepharoptosis
192900 Vertebral Hypoplasia with Lumbar Kyphosis
192950 Vertical Talus, Congenital; CVT
613106 Vertigo, Benign Recurrent, 2; BRV2
193007 Vertigo, Benign Recurrent; BRV
193000 Vesicoureteral Reflux 1; VUR1 (1 mouse models)
610878 Vesicoureteral Reflux 2; VUR2
613674 Vesicoureteral Reflux 3; VUR3
614317 Vesicoureteral Reflux 4; VUR4
614318 Vesicoureteral Reflux 5; VUR5
614319 Vesicoureteral Reflux 6; VUR6
615390 Vesicoureteral Reflux 7; VUR7
615963 Vesicoureteral Reflux 8; VUR8
314550 Vesicoureteral Reflux, X-Linked; VURX
193005 Vestibulocochlear Dysfunction, Progressive
125630 Vibratory Urticaria; VBU
242840 Vici Syndrome; VICIS
193070 Virus Rd114 RNA Complementarity
277320 Visceral Myopathy, Familial, with External Ophthalmoplegia
155310 Visceral Myopathy; VSCM (1 mouse models)
609629 Visceral Neuropathy, Familial, Autosomal Dominant
243180 Visceral Neuropathy, Familial, Autosomal Recessive (1 mouse models)
228100 Visceral Steatosis, Congenital (1 mouse models)
277440 Vitamin D-Dependent Rickets, Type 2A; VDDR2A (4 mouse models)
600785 Vitamin D-Dependent Rickets, Type 2b, with Normal Vitamin D Receptor;
264700 Vitamin D Hydroxylation-Deficient Rickets, Type 1A; VDDR1A (2 mouse models)
600081 Vitamin D Hydroxylation-Deficient Rickets, Type 1B; VDDR1B
277460 Vitamin E, Familial Isolated Deficiency Of; VED (3 mouse models)
277450 Vitamin K-Dependent Clotting Factors, Combined Deficiency of, 1; VKCFD1
607473 Vitamin K-Dependent Clotting Factors, Combined Deficiency of, 2; VKCFD2
606579 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1;
193200 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6;
277465 Vitiligo, Progressive, with Mental Retardation and Urethral Duplication
193230 Vitreoretinal Degeneration, Snowflake Type; SVD
193220 Vitreoretinochoroidopathy; VRCP
193235 Vitreoretinopathy, Neovascular Inflammatory; VRNI
193240 Vocal Cord Paralysis and Ptosis
604117 Vohwinkel Syndrome, Variant Form
124500 Vohwinkel Syndrome; VOWNKL
193250 Volvulus of Midgut
193300 Von Hippel-Lindau Syndrome; VHL (17 mouse models)
193400 Von Willebrand Disease, Type 1; VWD1 (1 mouse models)
613554 Von Willebrand Disease, Type 2; VWD2
277480 Von Willebrand Disease, Type 3; VWD3
314560 Von Willebrand Disease, X-Linked Form
193450 Vulvovaginitis, Allergic Seminal

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last database update
MGI 6.07
The Jackson Laboratory