Online Directory

Section 1A

Disorders MIM Genes MIM Specialties Commissioning
Waardenburg Syndrome, Type 1; WS1 193500
paired box 3; PAX3 606597
  • Audiology, Adult
  • Clinical Genetics
Waardenburg Syndrome, Type 3; WS3 148820
paired box 3; PAX3 606597
  • Audiology, Adult
  • Clinical Genetics
Wagner Vitreoretinopathy; WGVRP 143200
versican; VCAN 118661
  • Clinical Genetics
  • Ophthalmology, Adult
  • Ophthalmology, Paediatric
Warburg Micro Syndrome 1; WARBM1 600118
RAB3 GTPase activating protein catalytic subunit 1; RAB3GAP1 602536
  • Clinical Genetics
Weaver Syndrome; WVS 277590
enhancer of zeste 2 polycomb repressive complex 2 subunit; EZH2 601573
  • Clinical Genetics
Weissenbacher-Zweymuller Syndrome; WZS 277610
collagen, type XI, alpha 2; COL11A2 120290
  • Clinical Genetics
  • Ophthalmology, Adult
  • Ophthalmology, Paediatric
Wilms Tumor 1; WT1 194070
Wilms tumor 1; WT1 607102
  • Clinical Genetics
  • Oncology, Paediatric
Wilms Tumor 2; WT2 194071
H19, imprinted maternally expressed transcript (non-protein coding); H19 103280
insulin-like growth factor 2; IGF2 147470
  • Clinical Genetics
  • Oncology, Paediatric
Wilms Tumor, Aniridia, Genitourinary Anomalies, And Mental Retardation Syndrome; WAGR 194072
paired box 6; PAX6 607108
  • Clinical Genetics
Wilson Disease 277900
ATPase copper transporting beta; ATP7B 606882
  • Hepatology, Adult

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