Disorders
0-9 | 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
- Waardenburg Syndrome Type I GeneReviewOMIM
- Waardenburg Syndrome Type II OMIM
- Waardenburg Syndrome Type IIA OMIM
- Waardenburg Syndrome Type IIB OMIM
- Waardenburg Syndrome Type IIC OMIM
- Waardenburg Syndrome Type IID OMIM
- Waardenburg Syndrome Type IIE OMIM
- Waardenburg Syndrome Type III OMIM
- Waardenburg Syndrome Type IVA OMIM
- Waardenburg Syndrome Type IVB OMIM
- Waardenburg Syndrome Type IVC OMIM
- Warburg Micro Syndrome 1 OMIM
- Warburg Micro Syndrome 2 OMIM
- Warburg Micro Syndrome 3 OMIM
- WAS-Related Disorders GeneReviewOMIM
- Wiskott-Aldrich Syndrome OMIM
- X-Linked Severe Congenital Neutropenia
- X-Linked Thrombocytopenia
- Watson Syndrome OMIM
- Weaver Syndrome 1 OMIM
- Weill-Marchesani Syndrome GeneReviewOMIM
- ADAMTS10-Related Weill-Marchesani Syndrome OMIM
- FBN1-Related Weill-Marchesani Syndrome OMIM
- LTBP2-Related Weill-Marchesani Syndrome OMIM
- Weill-Marchesani-Like Syndrome OMIM
- Weissenbacher-Zweymuller Syndrome OMIM
- Werner Syndrome GeneReviewOMIM
- Weyers Acrofacial Dysostosis OMIM
- WFS1-Related Disorders GeneReviewOMIM
- DFNA6/14/38 Nonsyndromic Low Frequency Sensorineural Hearing Loss OMIM
- Wolfram Syndrome OMIM
- Wolfram Syndrome-Like Disease OMIM
- White Sponge Nevus of Cannon, KRT13-Related OMIM
- White Sponge Nevus of Cannon, KRT4-Related OMIM
- Williams Syndrome GeneReviewOMIM
- Williams-Beuren Region Duplication Syndrome OMIM
- Wilms Tumor GeneReviewOMIM
- Wilson Disease GeneReviewOMIM
- Winchester Syndrome OMIM
- Witkop Syndrome OMIM
- WNT5A-Related Robinow Syndrome, Autosomal Dominant OMIM
- Wolf-Hirschhorn Syndrome GeneReviewOMIM
- Pitt-Rogers-Danks Syndrome
- Wolff-Parkinson-White Syndrome OMIM
- Wolfram Syndrome 2 OMIM
- X-Linked Adrenal Hypoplasia Congenita GeneReviewOMIM
- Complex Glycerol Kinase Deficiency OMIM
- Isolated X-Linked Adrenal Hypoplasia Congenita OMIM
- X-Linked Agammaglobulinemia GeneReviewOMIM
- X-Linked Centronuclear Myopathy GeneReviewOMIM
- X-linked Cone-Rod Dystrophy 3 OMIM
- X-Linked Dystonia-Parkinsonism Syndrome GeneReviewOMIM
- X-Linked Hyper IgM Syndrome GeneReviewOMIM
- X-Linked Hypophosphatemia GeneReviewOMIM
- X-Linked Juvenile Retinoschisis GeneReviewOMIM
- X-Linked Leigh Syndrome OMIM
- X-Linked Mental Retardation 17 OMIM
- X-Linked Mental Retardation 19 OMIM
- X-Linked Mental Retardation 21 OMIM
- X-Linked Mental Retardation 30 OMIM
- X-Linked Mental Retardation 41 OMIM
- X-Linked Mental Retardation 45 OMIM
- X-Linked Mental Retardation 46 OMIM
- X-Linked Mental Retardation 58 OMIM
- X-linked Mental Retardation 59 OMIM
- X-Linked Mental Retardation 63 OMIM
- X-Linked Mental Retardation 72 OMIM
- X-Linked Mental Retardation 88 OMIM
- X-Linked Mental Retardation 89 OMIM
- X-Linked Mental Retardation 9 OMIM
- X-Linked Mental Retardation 90 OMIM
- X-Linked Mental Retardation 91 OMIM
- X-Linked Mental Retardation 93 OMIM
- X-Linked Mental Retardation 94 OMIM
- X-Linked Mental Retardation 95 OMIM
- X-Linked Mental Retardation Associated with Fragile Site FRAXE OMIM
- X-Linked Mental Retardation with Cerebellar Hypoplasia and Distinctive Facial Appearance OMIM
- X-Linked Mental Retardation with Epilepsy OMIM
- X-linked Mental Retardation, Nonspecific
- X-Linked Protoporphyria GeneReviewOMIM
- X-Linked Severe Combined Immunodeficiency GeneReviewOMIM
- X-Linked Sideroblastic Anemia OMIM
- X-Linked Sideroblastic Anemia and Ataxia GeneReviewOMIM
- X-Linked Syndromic Mental Retardation 10 OMIM
- X-Linked Syndromic Mental Retardation 13 OMIM
- X-Linked Syndromic Mental Retardation, Claes-Jensen Type OMIM
- Xanthinuria, Type I OMIM
- Xeroderma Pigmentosum GeneReviewOMIM
- DDB2-Related Xeroderma Pigmentosum OMIM
- ERCC1-Related Xeroderma Pigmentosum OMIM
- ERCC2-Related Xeroderma Pigmentosum OMIM
- ERCC3-Related Xeroderma Pigmentosum OMIM
- ERCC4-Related Xeroderma Pigmentosum OMIM
- ERCC5-Related Xeroderma Pigmentosum OMIM
- POLH-Related Xeroderma Pigmentosum OMIM
- XPA-Related Xeroderma Pigmentosum OMIM
- XPC-Related Xeroderma Pigmentosum OMIM
- Xeroderma Pigmentosum Multi-Gene Panels
- Xp11.3 Deletion Syndrome OMIM





