Testing Criteria

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Testing criteria Disorders Genes Date
Vacterl Association, X-Linked, With Or Without Hydrocephalus
  • Vacterl Association, X-Linked, With Or Without Hydrocephalus
    • Vacterl Association With Hydrocephalus, X-Linked
    • Vacterl-H, X-Linked
  • fanconi anemia, complementation group B
    • fanconi anaemia, complementation group B
    • fanconi anaemia-associated polypeptide, 95-kd
    • fanconi anemia-associated polypeptide, 95-kd
2008
Ventricular Tachycardia, Catecholaminergic Polymorphic, 1, With Or Without Atrial Dysfunction And/or Dilated Cardiomyopathy
  • Ventricular Tachycardia, Catecholaminergic Polymorphic, 1, With Or Without Atrial Dysfunction And/or Dilated Cardiomyopathy
    • Ventricular Tachycardia, Stress-Induced Polymorphic
  • ryanodine receptor 2
    • arrhythmogenic right ventricular dysplasia 2
    • ryanodine receptor 2 (cardiac)
    • ryanodine receptor, cardiac
2008
Ventricular Tachycardias, Catecholaminergic Polymorphic, 5 Gene Panel
  • Arrhythmogenic Right Ventricular Dysplasia, Familial, 2
    • Arrhythmogenic Right Ventricular Cardiomyopathy 2
  • Atrial Fibrillation, Familial, 9
  • Short QT Syndrome 3
  • Ventricular Tachycardia, Catecholaminergic Polymorphic, 1, With Or Without Atrial Dysfunction And/or Dilated Cardiomyopathy
    • Ventricular Tachycardia, Stress-Induced Polymorphic
  • Ventricular Tachycardia, Catecholaminergic Polymorphic, 2
    • Ventricular Tachycardia, Stress-Induced Polymorphic
  • Ventricular Tachycardia, Catecholaminergic Polymorphic, 4
  • Ventricular Tachycardia, Catecholaminergic Polymorphic, 5, With Or Without Muscle Weakness
  • calmodulin 1
    • calmodulin 1 (phosphorylase kinase, delta)
  • calsequestrin 2
    • calsequestrin 2 (cardiac muscle)
  • potassium voltage-gated channel subfamily J member 2
    • potassium inwardly-rectifying channel, subfamily J, member 2
  • ryanodine receptor 2
    • arrhythmogenic right ventricular dysplasia 2
    • ryanodine receptor 2 (cardiac)
    • ryanodine receptor, cardiac
  • triadin
2014
Vici Syndrome
  • Vici Syndrome
    • Immunodeficiency With Cleft Lip/Palate, Cataract, Hypopigmentation, And Absent Corpus Callosum
  • ectopic P-granules autophagy protein 5 homolog
    • ectopic P-granules autophagy protein 5 homolog (C. elegans)
    • ectopic p-granules autophagy protein 5, c. elegans, homolog of
2013
Von Hippel-Lindau Syndrome
  • Von Hippel-Lindau Syndrome
    • Von Hippel Lindau
  • von Hippel-Lindau tumor suppressor
    • VHL gene
    • von hippel-lindau syndrome
    • von hippel-lindau tumor suppressor
    • Von Hippel-Lindau tumor suppressor, E3 ubiquitin protein ligase
2011

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