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Human Disease Vocabulary Browser
The current vocabulary contains human disease, syndrome, and condition terms from Online Mendelian Inheritance in Man (OMIM database).

Browse vocabulary terms by beginning character
 
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Human Diseases/Syndromes Beginning with "W"

To see all annotations for a disease, click the disease name.

OMIM IDHuman Disease
193500 Waardenburg Syndrome, Type 1; WS1 (7 mouse models)
193510 Waardenburg Syndrome, Type 2A; WS2A (13 mouse models)
600193 Waardenburg Syndrome, Type 2B; WS2B
606662 Waardenburg Syndrome, Type 2c; WS2C
608890 Waardenburg Syndrome, Type 2D; WS2D (1 mouse models)
611584 Waardenburg Syndrome, Type 2E; WS2E
148820 Waardenburg Syndrome, Type 3; WS3
277580 Waardenburg Syndrome, Type 4A; WS4A (2 mouse models)
613265 Waardenburg Syndrome, Type 4b; WS4B (3 mouse models)
613266 Waardenburg Syndrome, Type 4c; WS4C
143200 Wagner Vitreoretinopathy; WGVRP
615170 Wahab Syndrome
600118 Warburg Micro Syndrome 1; WARBM1
614225 Warburg Micro Syndrome 2; WARBM2
614222 Warburg Micro Syndrome 3; WARBM3
615663 Warburg Micro Syndrome 4; WARBM4 (1 mouse models)
613398 Warsaw Breakage Syndrome; WABS
193520 Watson Syndrome
277590 Weaver Syndrome; WVS
615926 Webb-Dattani Syndrome; WEDAS
608710 Wegener Granulomatosis
613195 Weill-Marchesani-Like Syndrome
277600 Weill-Marchesani Syndrome 1; WMS1
608328 Weill-Marchesani Syndrome 2; WMS2 (2 mouse models)
614819 Weill-Marchesani Syndrome 3; WMS3
112350 Weismann-Netter Syndrome; WNS
277610 Weissenbacher-Zweymuller Syndrome; WZS
604454 Welander Distal Myopathy; WDM
277700 Werner Syndrome; WRN (3 mouse models)
277730 Wernicke-Korsakoff Syndrome
610379 West Nile Virus, Susceptibility to
193530 Weyers Acrofacial Dysostosis; WAD
602418 Weyers Ulnar Ray/Oligodactyly Syndrome
193670 WHIM Syndrome (1 mouse models)
277720 Whistling Face Syndrome, Recessive Form
277740 White Forelock with Malformations
193900 White Sponge Nevus 1; WSN1 (2 mouse models)
615785 White Sponge Nevus 2; WSN2
194000 Widow's Peak
314570 Widow's Peak Syndrome
314580 Wieacker-Wolff Syndrome; WRWF
314600 Wildervanck Syndrome
609757 Williams-Beuren Region Duplication Syndrome
194050 Williams-Beuren Syndrome; WBS (17 mouse models)
194070 Wilms Tumor 1; WT1
194071 Wilms Tumor 2; WT2
194090 Wilms Tumor 3; WT3
601363 Wilms Tumor 4
601583 Wilms Tumor 5; WT5
194072 Wilms Tumor, Aniridia, Genitourinary Anomalies, and Mental Retardation Syndrome; WAGR
612469 Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, and Obesity Syndrome; WAGRO
277900 Wilson Disease (3 mouse models)
309585 Wilson-Turner X-Linked Mental Retardation Syndrome; WTS
277950 Winchester Syndrome; WNCHRS
277970 Wiskott-Aldrich Syndrome
614493 Wiskott-Aldrich Syndrome 2; WAS2
600903 Wiskott-Aldrich Syndrome, Autosomal Dominant Form
301000 Wiskott-Aldrich Syndrome; WAS (3 mouse models)
189500 Witkop Syndrome
300421 Wittwer Syndrome
277990 Wolff Mental Retardation Syndrome
194200 Wolff-Parkinson-White Syndrome (4 mouse models)
194190 Wolf-Hirschhorn Syndrome; WHS (7 mouse models)
614296 Wolfram-Like Syndrome, Autosomal Dominant; WFSL
222300 Wolfram Syndrome 1; WFS1 (3 mouse models)
604928 Wolfram Syndrome 2; WFS2 (1 mouse models)
598500 Wolfram Syndrome, Mitochondrial Form
278100 Wolman Disease with Hypolipoproteinemia and Acanthocytosis
241080 Woodhouse-Sakati Syndrome
615236 Woods Syndrome
194300 Woolly Hair, Autosomal Dominant; ADWH
278200 Woolly Hair, Hypotrichosis, Everted Lower Lip, and Outstanding Ears
194320 Woronets Trait
278250 Wrinkly Skin Syndrome; WSS
194350 WT Limb-Blood Syndrome

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
10/21/2014
MGI 5.20
The Jackson Laboratory