| OMIM ID |
Human Disease |
| 276950 |
Vacterl Association with Hydrocephalus (2 mouse models) |
| 314390 |
Vacterl Association, X-Linked, with or without Hydrocephalus; VACTERLX |
| 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 |
| 604547 |
Van Der Woude Syndrome 1, Modifier of |
| 119300 |
Van Der Woude Syndrome 1; VWS1 (1 mouse model) |
| 606713 |
Van Der Woude Syndrome 2; VWS2 |
| 603570 |
Vanin 1; VNN1 |
| 600670 |
Varicella, Severe Recurrent |
| 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 |
| 192350 |
Vater Association (2 mouse models) |
| 608406 |
Vater-Like Defects with Pulmonary Hypertension, Laryngeal Webs, and Growth Deficiency |
| 192400 |
Veins, Pattern of, on Anterior Thorax |
| 192430 |
Velocardiofacial Syndrome (10 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 During Myocardial Infarction, Susceptibility to |
| 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 (4 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 |
| 192605 |
Ventricular Tachycardia, Familial |
| 219730 |
Ventriculomegaly with Cystic Kidney Disease |
| 602200 |
Ventriculomegaly with Defects of the Radius and Kidney |
| 192700 |
Venular Insufficiency, Systemic |
| 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 model) |
| 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 |
| 314550 |
Vesicoureteral Reflux, X-Linked; VURX |
| 193005 |
Vestibulocochlear Dysfunction, Progressive |
| 193050 |
Vibratory Angioedema |
| 242840 |
Vici Syndrome; VICIS |
| 193060 |
Vimentin; VIM |
| 193070 |
Virus Rd114 RNA Complementarity |
| 277320 |
Visceral Myopathy, Familial, with External Ophthalmoplegia |
| 609629 |
Visceral Neuropathy, Familial, Autosomal Dominant |
| 243180 |
Visceral Neuropathy, Familial, Autosomal Recessive (1 mouse model) |
| 228100 |
Visceral Steatosis, Congenital (1 mouse model) |
| 612542 |
Vitamin B12 Plasma Level Quantitative Trait Locus 1; B12QTL1 |
| 277440 |
Vitamin D-Dependent Rickets, Type 2A; VDDR2A (3 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 |
| 193250 |
Volvulus of Midgut |
| 193300 |
Von Hippel-Lindau Syndrome; VHL (17 mouse models) |
| 193400 |
Von Willebrand Disease, Type 1; VWD1 (1 mouse model) |
| 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 |
Analysis Tools