Testing Criteria

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Testing criteria Disorders Genes Date
Waardenburg Syndrome Types 1 And 3
  • Waardenburg Syndrome, Type 1
    • Waardenburg Syndrome With Dystopia Canthorum
  • Waardenburg Syndrome, Type 3
    • Klein-Waardenburg Syndrome
    • Waardenburg Syndrome With Upper Limb Anomalies
    • Waardenburg Syndrome, Type III
  • paired box 3
    • paired domain gene hup2
2010
Wagner Syndrome 1
  • Wagner Vitreoretinopathy
    • Erosive VItreoretinopathy
    • Hyaloideoretinal Degeneration Of Wagner
    • Wagner Syndrome 1
    • Wagner VItreoretinal Degeneration
  • versican
    • chondroitin sulfate proteoglycan 2
    • chondroitin sulfate proteoglycan core protein, cartilage
    • versican proteoglycan
2011
Warburg Micro Syndrome 1
  • Warburg Micro Syndrome 1
    • Micro Syndrome
  • RAB3 GTPase activating protein catalytic subunit 1
    • RAB3 GTPase activating protein subunit 1 (catalytic)
    • RAB3GAP, 130-kD subunit
    • RAB3GAP, catalytic subunit
    • WARBM1 gene
2013
Weaver Syndrome
  • Weaver Syndrome
    • Weaver-Like Syndrome, Included
    • Weaver-Smith Syndrome
  • enhancer of zeste 2 polycomb repressive complex 2 subunit
    • enhancer of zeste (Drosophila) homolog 2
    • enhancer of zeste homolog 2 (Drosophila)
2012
Wilms Tumor 2
  • Wilms Tumor 2
  • H19, imprinted maternally expressed transcript (non-protein coding)
    • H19, imprinted maternally expressed transcript h19
    • H19, imprinted maternally expressed untranslated mRNA
  • insulin-like growth factor 2
    • insulin-like growth factor 2 (somatomedin a)
    • somatomedin a
2008
WNT10A Related Disorders
  • Odontoonychodermal Dysplasia
  • Wnt family member 10A
    • wingless-type MMTV integration site family, member 10A
2011
WNT10A Related Disorders
  • Schopf-Schulz-Passarge Syndrome
    • Eccrine Tumors With Ectodermal Dysplasia
    • Keratosis Palmoplantaris With Cystic Eyelids, Hypodontia, And Hypotrichosis
  • Wnt family member 10A
    • wingless-type MMTV integration site family, member 10A
2011

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