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 ID	Human 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:611584	Waardenburg Syndrome, Type 2E; WS2E
OMIM:619947	Waardenburg Syndrome, Type 2F; WS2F
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:612469	Wagro Syndrome; WAGRO
OMIM:615170	Wahab Syndrome
OMIM:311510	Waisman Syndrome; WSMN
OMIM:618175	Warburg-Cinotti Syndrome; WRCN
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:301052	Warfarin Sensitivity, X-Linked
OMIM:613398	Warsaw Breakage Syndrome; WABS
OMIM:193520	Watson Syndrome; WTSN
OMIM:277590	Weaver Syndrome; WVS
OMIM:615926	Webb-Dattani Syndrome; WEDAS
OMIM:277600	Weill-Marchesani Syndrome 1; WMS1
OMIM:608328	Weill-Marchesani Syndrome 2; WMS2
OMIM:614819	Weill-Marchesani Syndrome 3; WMS3
OMIM:613195	Weill-Marchesani Syndrome 4; WMS4
OMIM:112350	Weismann-Netter Syndrome; WNS
OMIM:618619	Weiss-Kruszka Syndrome; WSKA
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 1; WHIMS1
OMIM:619407	Whim Syndrome 2; WHIMS2
OMIM:277720	Whistling Face Syndrome, Recessive Form
OMIM:277740	White Forelock with Malformations
OMIM:619426	White-Kernohan Syndrome; WHIKERS
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:301041	Wieacker-Wolff Syndrome, Female-Restricted; WRWFFR
OMIM:314580	Wieacker-Wolff Syndrome; WRWF
OMIM:264090	Wiedemann-Rautenstrauch Syndrome; WDRTS
OMIM:605130	Wiedemann-Steiner Syndrome; WDSTS
OMIM:314600	Wildervanck Syndrome
OMIM:609757	Williams-Beuren Region Duplication Syndrome
OMIM:194050	Williams-Beuren Syndrome; WBS
OMIM:211450	Williams-Campbell Syndrome
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 Impaired Intellectual Development Syndrome; WAGR
OMIM:277900	Wilson Disease; WND
OMIM:277950	Winchester Syndrome; WNCHRS
OMIM:614493	Wiskott-Aldrich Syndrome 2; WAS2
OMIM:600903	Wiskott-Aldrich Syndrome, Autosomal Dominant
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; WPW
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:620151	Wolman Disease; WOLD
OMIM:241080	Woodhouse-Sakati Syndrome; WDSKS
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:620415	Woolly Hair-Skin Fragility Syndrome; WHSF
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 Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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