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DisGeNET
DisGeNET is a knowledge management platform that integrates and standardizes the data of genes and mutations related to diseases from multiple sources. It covers entire range of human disease.
| Source | Last Updated |
|---|---|
| DisGeNET | July 29, 2024 |
| Disease ID | Disease Name | Gene Symbol | Gene ID | Gene Name | UniProt ID ▲ |
|---|---|---|---|---|---|
| C0018051 | Gonadal Dysgenesis | RXYLT1 | 10329 | ribitol xylosyltransferase 1 | Q9Y2B1 |
| C0026010 | Microphthalmos | RXYLT1 | 10329 | ribitol xylosyltransferase 1 | Q9Y2B1 |
| C0282577 | Congenital Disorders of Glycosylation | RXYLT1 | 10329 | ribitol xylosyltransferase 1 | Q9Y2B1 |
| C0010038 | Corneal Opacity | RXYLT1 | 10329 | ribitol xylosyltransferase 1 | Q9Y2B1 |
| C0036572 | Seizures | RXYLT1 | 10329 | ribitol xylosyltransferase 1 | Q9Y2B1 |
| C0026850 | Muscular Dystrophy | RXYLT1 | 10329 | ribitol xylosyltransferase 1 | Q9Y2B1 |
| C0010417 | Cryptorchidism | RXYLT1 | 10329 | ribitol xylosyltransferase 1 | Q9Y2B1 |
| C1836373 | MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2K | RXYLT1 | 10329 | ribitol xylosyltransferase 1 | Q9Y2B1 |
| C0854723 | Retinal Dystrophies | RXYLT1 | 10329 | ribitol xylosyltransferase 1 | Q9Y2B1 |
| C0086543 | Cataract | RXYLT1 | 10329 | ribitol xylosyltransferase 1 | Q9Y2B1 |
| C0035305 | Retinal Detachment | RXYLT1 | 10329 | ribitol xylosyltransferase 1 | Q9Y2B1 |
| C4284790 | Muscular Dystrophy-Dystroglycanopathy (Congenital with Brain and Eye Anomalies) Type A, 1 | RXYLT1 | 10329 | ribitol xylosyltransferase 1 | Q9Y2B1 |
| C0025958 | Microcephaly | RXYLT1 | 10329 | ribitol xylosyltransferase 1 | Q9Y2B1 |
| C0020255 | Hydrocephalus | RXYLT1 | 10329 | ribitol xylosyltransferase 1 | Q9Y2B1 |
| C0008925 | Cleft Palate | PIGL | 9487 | phosphatidylinositol glycan anchor biosynthesis class L | Q9Y2B2 |
| C0002736 | Amyotrophic Lateral Sclerosis | PIGL | 9487 | phosphatidylinositol glycan anchor biosynthesis class L | Q9Y2B2 |
| C0037299 | Skin Ulcer | PIGL | 9487 | phosphatidylinositol glycan anchor biosynthesis class L | Q9Y2B2 |
| C0039685 | Tetralogy of Fallot | PIGL | 9487 | phosphatidylinositol glycan anchor biosynthesis class L | Q9Y2B2 |
| C0004352 | Autistic Disorder | PIGL | 9487 | phosphatidylinositol glycan anchor biosynthesis class L | Q9Y2B2 |
| C0221356 | Brachycephaly | PIGL | 9487 | phosphatidylinositol glycan anchor biosynthesis class L | Q9Y2B2 |
| C0019569 | Hirschsprung Disease | PIGL | 9487 | phosphatidylinositol glycan anchor biosynthesis class L | Q9Y2B2 |
| C0014877 | Esotropia | PIGL | 9487 | phosphatidylinositol glycan anchor biosynthesis class L | Q9Y2B2 |
| C0023449 | Acute lymphocytic leukemia | PIGL | 9487 | phosphatidylinositol glycan anchor biosynthesis class L | Q9Y2B2 |
| C0027066 | Myoclonus | PIGL | 9487 | phosphatidylinositol glycan anchor biosynthesis class L | Q9Y2B2 |
| C0020608 | Hypodontia | PIGL | 9487 | phosphatidylinositol glycan anchor biosynthesis class L | Q9Y2B2 |
