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 ID	Human Disease
OMIM:276950	Vacterl Association with Hydrocephalus
OMIM:314390	Vacterl Association, X-Linked, with or without Hydrocephalus;
OMIM:277100	Valinemia
OMIM:609442	Valproate Embryopathy, Susceptibility to
OMIM:277150	Van Bogaert-Hozay Syndrome
OMIM:239100	Van Buchem Disease; VBCH
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:301030	Van Esch-O'driscoll Syndrome; VEODS
OMIM:601390	Van Maldergem Syndrome 1; VMLDS1
OMIM:615546	Van Maldergem Syndrome 2; VMLDS2
OMIM:600670	Varicella, Severe Recurrent
OMIM:192200	Varicose Veins
OMIM:620483	Variegate Porphyria, Childhood-Onset; VPCO
OMIM:176200	Variegate Porphyria; VP
OMIM:192300	Vascular Helix of Umbilical Cord
OMIM:277175	Vascular Hyalinosis
OMIM:606893	Vascular Malformation, Primary Intraosseous; VMPI
OMIM:615688	Vasculitis, Autoinflammation, Immunodeficiency, and Hematologic Defects Syndrome; VAIHS
OMIM:609817	Vasculitis, Lymphocytic, Cutaneous Small Vessel
OMIM:192310	Vasculitis, Lymphocytic, Nodular
OMIM:192315	Vasculopathy, Retinal, with Cerebral Leukoencephalopathy and Systemic Manifestations; RVCLS
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; VCFS
OMIM:600736	Velofacioskeletal Syndrome
OMIM:600195	Venous Malformations, Multiple Cutaneous and Mucosal; VMCM
OMIM:115000	Ventricular Arrhythmias Due to Cardiac Ryanodine Receptor Calcium Release Deficiency Syndrome; VACRDS
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:192605	Ventricular Tachycardia, Familial
OMIM:619501	Ventriculomegaly and Arthrogryposis; VENARG
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:618223	Vertebral Anomalies and Variable Endocrine and T-Cell Dysfunction;
OMIM:617660	Vertebral, Cardiac, Renal, and Limb Defects Syndrome 1; VCRL1
OMIM:617661	Vertebral, Cardiac, Renal, and Limb Defects Syndrome 2; VCRL2
OMIM:618845	Vertebral, Cardiac, Renal, and Limb Defects Syndrome 3; VCRL3
OMIM:619227	Vertebral, Cardiac, Tracheoesophageal, Renal, and Limb Defects;
OMIM:192800	Vertebral Fusion, Posterior Lumbosacral, with Blepharoptosis
OMIM:619122	Vertebral Hypersegmentation and Orofacial Anomalies; VHO
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:617982	Ververi-Brady Syndrome; VERBRAS
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:301054	Vexas Syndrome; VEXAS
OMIM:125630	Vibratory Urticaria; VBU
OMIM:242840	Vici Syndrome; VICIS
OMIM:193070	Virus Rd114 RNA Complementarity
OMIM:619400	Visceral Leiomyopathy, African Degenerative; ADL
OMIM:155310	Visceral Myopathy 1; VSCM1
OMIM:619350	Visceral Myopathy 2; VSCM2
OMIM:277320	Visceral Myopathy, Familial, with External Ophthalmoplegia
OMIM:243180	Visceral Neuropathy, Familial, 1, Autosomal Recessive; VSCN1
OMIM:619465	Visceral Neuropathy, Familial, 2, Autosomal Recessive; VSCN2
OMIM:609629	Visceral Neuropathy, Familial, 3, Autosomal Dominant; VSCN3
OMIM:228100	Visceral Steatosis, Congenital
OMIM:619033	Vissers-Bodmer Syndrome; VIBOS
OMIM:619472	Viss Syndrome; VISS
OMIM:618283	Visual Impairment and Progressive Phthisis Bulbi; VIPB
OMIM:277440	Vitamin D-Dependent Rickets, Type 2A; VDDR2A
OMIM:600785	Vitamin D-Dependent Rickets, Type 2b, with Normal Vitamin D Receptor;
OMIM:619073	Vitamin D-Dependent Rickets, Type 3; VDDR3
OMIM:264700	Vitamin D Hydroxylation-Deficient Rickets, Type 1A; VDDR1A
OMIM:600081	Vitamin D Hydroxylation-Deficient Rickets, Type 1B; VDDR1B
OMIM:277450	Vitamin K-Dependent Clotting Factors, Combined Deficiency of, 1;
OMIM:607473	Vitamin K-Dependent Clotting Factors, Combined Deficiency of, 2;
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:619248	Vitreoretinopathy with Phalangeal Epiphyseal Dysplasia; VPED
OMIM:193240	Vocal Cord Paralysis and Ptosis
OMIM:604117	Vohwinkel Syndrome, Variant Form
OMIM:124500	Vohwinkel Syndrome; VOWNKL
OMIM:610030	Voltage-Dependent Anion Channel 1 Pseudogene 4; VDAC1P4
OMIM:193250	Volvulus of Midgut
OMIM:193300	Von Hippel-Lindau Syndrome; VHLS
OMIM:177820	Von Willebrand Disease, Platelet-Type; VWDP
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:615828	Vulto-Van Silfhout-De Vries Syndrome; VSVS
OMIM:193450	Vulvovaginitis, Allergic Seminal

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