About   Help   FAQ
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
 
A B C D E F G H I J K L M N O P Q R S T U V W X Y Z 0-9
 

Human Diseases/Syndromes Beginning with "W"

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

OMIM IDHuman Disease
OMIM:193500 Waardenburg Syndrome, Type 1; WS1
OMIM:193510 Waardenburg Syndrome, Type 2A; WS2A
OMIM:600193 Waardenburg Syndrome, Type 2B; WS2B
OMIM:606662 Waardenburg Syndrome, Type 2c; WS2C
OMIM:608890 Waardenburg Syndrome, Type 2D; WS2D
OMIM:611584 Waardenburg Syndrome, Type 2E; WS2E
OMIM:148820 Waardenburg Syndrome, Type 3; WS3
OMIM:277580 Waardenburg Syndrome, Type 4A; WS4A
OMIM:613265 Waardenburg Syndrome, Type 4b; WS4B
OMIM:613266 Waardenburg Syndrome, Type 4c; WS4C
OMIM:143200 Wagner Vitreoretinopathy; WGVRP
OMIM:615170 Wahab Syndrome
OMIM:311510 Waisman Syndrome; WSMN
OMIM:600118 Warburg Micro Syndrome 1; WARBM1
OMIM:614225 Warburg Micro Syndrome 2; WARBM2
OMIM:614222 Warburg Micro Syndrome 3; WARBM3
OMIM:615663 Warburg Micro Syndrome 4; WARBM4
OMIM:613398 Warsaw Breakage Syndrome; WABS
OMIM:193520 Watson Syndrome; WTSN
OMIM:277590 Weaver Syndrome; WVS
OMIM:615926 Webb-Dattani Syndrome; WEDAS
OMIM:608710 Wegener Granulomatosis
OMIM:613195 Weill-Marchesani-Like Syndrome
OMIM:277600 Weill-Marchesani Syndrome 1; WMS1
OMIM:608328 Weill-Marchesani Syndrome 2; WMS2
OMIM:614819 Weill-Marchesani Syndrome 3; WMS3
OMIM:112350 Weismann-Netter Syndrome; WNS
OMIM:604454 Welander Distal Myopathy; WDM
OMIM:277700 Werner Syndrome; WRN
OMIM:277730 Wernicke-Korsakoff Syndrome
OMIM:610379 West Nile Virus, Susceptibility to
OMIM:193530 Weyers Acrofacial Dysostosis; WAD
OMIM:602418 Weyers Ulnar Ray/Oligodactyly Syndrome
OMIM:193670 Whim Syndrome; WHIMS
OMIM:277720 Whistling Face Syndrome, Recessive Form
OMIM:277740 White Forelock with Malformations
OMIM:193900 White Sponge Nevus 1; WSN1
OMIM:615785 White Sponge Nevus 2; WSN2
OMIM:616364 White-Sutton Syndrome; WHSUS
OMIM:194000 Widow's Peak
OMIM:314570 Widow's Peak Syndrome
OMIM:314580 Wieacker-Wolff Syndrome; WRWF
OMIM:605130 Wiedemann-Steiner Syndrome; WDSTS
OMIM:314600 Wildervanck Syndrome
OMIM:609757 Williams-Beuren Region Duplication Syndrome
OMIM:194050 Williams-Beuren Syndrome; WBS
OMIM:194070 Wilms Tumor 1; WT1
OMIM:194071 Wilms Tumor 2; WT2
OMIM:194090 Wilms Tumor 3; WT3
OMIM:601363 Wilms Tumor 4; WT4
OMIM:601583 Wilms Tumor 5; WT5
OMIM:616806 Wilms Tumor 6; WT6
OMIM:194072 Wilms Tumor, Aniridia, Genitourinary Anomalies, and Mental Retardation Syndrome; WAGR
OMIM:612469 Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, and Obesity Syndrome; WAGRO
OMIM:277900 Wilson Disease
OMIM:309585 Wilson-Turner X-Linked Mental Retardation Syndrome; WTS
OMIM:277950 Winchester Syndrome; WNCHRS
OMIM:277970 Wiskott-Aldrich Syndrome
OMIM:614493 Wiskott-Aldrich Syndrome 2; WAS2
OMIM:600903 Wiskott-Aldrich Syndrome, Autosomal Dominant Form
OMIM:301000 Wiskott-Aldrich Syndrome; WAS
OMIM:189500 Witkop Syndrome
OMIM:613406 Witteveen-Kolk Syndrome; WITKOS
OMIM:277990 Wolff Mental Retardation Syndrome
OMIM:194200 Wolff-Parkinson-White Syndrome
OMIM:194190 Wolf-Hirschhorn Syndrome; WHS
OMIM:614296 Wolfram-Like Syndrome, Autosomal Dominant; WFSL
OMIM:222300 Wolfram Syndrome 1; WFS1
OMIM:604928 Wolfram Syndrome 2; WFS2
OMIM:598500 Wolfram Syndrome, Mitochondrial Form
OMIM:278100 Wolman Disease with Hypolipoproteinemia and Acanthocytosis
OMIM:241080 Woodhouse-Sakati Syndrome
OMIM:615236 Woods Syndrome
OMIM:194300 Woolly Hair, Autosomal Dominant; ADWH
OMIM:616760 Woolly Hair, Autosomal Recessive 3; ARWH3
OMIM:278200 Woolly Hair, Hypotrichosis, Everted Lower Lip, and Outstanding Ears
OMIM:194320 Woronets Trait
OMIM:278250 Wrinkly Skin Syndrome; WSS
OMIM:194350 WT Limb-Blood Syndrome

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
Citing These Resources
Funding Information
Warranty Disclaimer & Copyright Notice
Send questions and comments to User Support.
last database update
09/12/2017
MGI 6.10
The Jackson Laboratory