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
- Udd Distal Myopathy GeneReviewOMIM
- Ulnar-Mammary Syndrome OMIM
- UMOD-Associated Kidney Disease GeneReviewOMIM
- Familial Juvenile Hyperuricemic Nephropathy Type 1 OMIM
- Medullary Cystic Kidney Disease 2
- UNC119-Related Cone-Rod Dystrophy OMIM
- Unverricht-Lundborg Disease GeneReviewOMIM
- UPK3A-Related Renal Adysplasia OMIM
- Urea Cycle Disorders GeneReview
- Arginase Deficiency GeneReviewOMIM
- Argininosuccinate Lyase Deficiency GeneReviewOMIM
- Argininosuccinic Aciduria
- Carbamoylphosphate Synthetase I Deficiency OMIM
- Citrullinemia Type I GeneReviewOMIM
- N-Acetylglutamate Synthase Deficiency OMIM
- Ornithine Transcarbamylase Deficiency OMIM
- UROD-Related Porphyrias GeneReviewOMIM
- Hepatoerythropoietic Porphyria
- UROD-Related Porphyria Cutanea Tarda
- Usher Syndrome Multi-Gene Panels
- Usher Syndrome Type 2 GeneReviewOMIM
- Usher Syndrome Type 2A OMIM
- Usher Syndrome Type 2C OMIM
- Usher Syndrome Type 2D OMIM
- Usher Syndrome Type 3 OMIM
- Usher Syndrome Type 3A OMIM
- Usher Syndrome Type 3B OMIM
- Usher Syndrome Type I GeneReviewOMIM
- Usher Syndrome Type 1B OMIM
- Usher Syndrome Type 1C OMIM
- Usher Syndrome Type 1D OMIM
- Usher Syndrome Type 1E OMIM
- Usher Syndrome Type 1F OMIM
- Usher Syndrome Type 1G OMIM
- Usher Syndrome Type 1H OMIM
- Usher Syndrome Type 1J OMIM
- Usher Syndrome Type 1K OMIM
- UV-Sensitive Syndrome 3 OMIM
- VACTERL Association with Hydrocephalus OMIM
- VACTERL Association, X-Linked, with or without Hydrocephalus OMIM
- VACTERL with Hydrocephalus, FANCB-Related OMIM
- Van Buchem Disease, Type 2 OMIM
- VANGL1-Related Neural Tube Defect OMIM
- VANGL2-Related Neural Tube Defect OMIM
- Variegate Porphyria GeneReviewOMIM
- Vascular Malformation Multi-Gene Panels
- VCAN-Related Vitreoretinopathy GeneReviewOMIM
- Erosive Vitreoretinopathy OMIM
- Wagner Syndrome OMIM
- Very Long Chain Acyl-Coenzyme A Dehydrogenase Deficiency GeneReviewOMIM
- Vesicoureteral Reflux 2 OMIM
- VHL-Related Pheochromocytoma OMIM
- Vitamin D-Dependent Rickets Type I OMIM
- Vitamin D-Dependent Rickets Type II OMIM
- Vitamin K-Dependent Clotting Factors, Combined Deficiency of, 1 OMIM
- Vitamin K-Dependent Clotting Factors, Combined Deficiency of, 2 OMIM
- Vitreoretinochoroidopathy OMIM
- VLDLR-Associated Cerebellar Hypoplasia GeneReviewOMIM
- Vohwinkel Syndrome OMIM
- Von Hippel-Lindau Disease GeneReviewOMIM
- von Willebrand Disease GeneReviewOMIM
- Type 1 von Willebrand Disease
- Type 2A von Willebrand Disease
- Type 2B von Willebrand Disease
- Type 2M von Willebrand Disease
- Type 2N von Willebrand Disease
- Type 3 von Willebrand Disease
- VSX2-Related Isolated Microphthalmia OMIM





