Online Directory

Section 1A

Disorders MIM Genes MIM Specialties Commissioning
Vacterl Association, X-Linked, With Or Without Hydrocephalus; VACTERLX 314390
fanconi anemia, complementation group B; FANCB 300515
  • Clinical Genetics
Van Der Woude Syndrome 1; VWS1 119300
interferon regulatory factor 6; IRF6 607199
  • Clinical Genetics
Ventricular Tachycardia, Catecholaminergic Polymorphic, 1, With Or Without Atrial Dysfunction And/or Dilated Cardiomyopathy; CPVT1 604772
ryanodine receptor 2; RYR2 180902
  • Cardiology, Adult
  • Cardiology, Paediatric
  • Clinical Genetics
Vici Syndrome; VICIS 242840
ectopic P-granules autophagy protein 5 homolog; EPG5 615068
  • Clinical Genetics
  • Immunology, Paediatric
  • Neurology, Paediatric
Vitreoretinochoroidopathy; VRCP 193220
bestrophin 1; BEST1 607854
  • Clinical Genetics
  • Ophthalmology, Adult
  • Ophthalmology, Paediatric
Von Hippel-Lindau Syndrome; VHL 193300
von Hippel-Lindau tumor suppressor; VHL 608537
  • Clinical Genetics
Von Willebrand Disease, Type 1; VWD1 193400
von Willebrand factor; VWF 613160
  • Haematology, Adult
  • Haematology, Paediatric
  • Prescribed Specialised Services
Von Willebrand Disease, Type 2; VWD2 613554
von Willebrand factor; VWF 613160
  • Haematology, Adult
  • Haematology, Paediatric
  • Prescribed Specialised Services
Von Willebrand Disease, Type 3; VWD3 277480
von Willebrand factor; VWF 613160
  • Haematology, Adult
  • Haematology, Paediatric
  • Prescribed Specialised Services

Section 1B

Disorders MIM Genes MIM Specialties Commissioning
Ventricular Tachycardias, Catecholaminergic Polymorphic, 5 Gene Panel 0
...see test listing on database for full details 0
  • Cardiology, Adult
  • Cardiology, Paediatric
  • Clinical Genetics
  • Clinical Commissioning Group
  • Prescribed Specialised Services

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