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 ▼ |
---|---|---|---|---|---|
C0014518 | Toxic Epidermal Necrolysis | SDHD | 6392 | succinate dehydrogenase complex subunit D | O14521 |
C0007134 | Renal Cell Carcinoma | SDHD | 6392 | succinate dehydrogenase complex subunit D | O14521 |
C1306459 | Primary malignant neoplasm | SDHD | 6392 | succinate dehydrogenase complex subunit D | O14521 |
C0456909 | Blindness | SDHD | 6392 | succinate dehydrogenase complex subunit D | O14521 |
C0021847 | Intestinal Pseudo-Obstruction | SDHD | 6392 | succinate dehydrogenase complex subunit D | O14521 |
C0015230 | Exanthema | SDHD | 6392 | succinate dehydrogenase complex subunit D | O14521 |
C1384666 | hearing impairment | SDHD | 6392 | succinate dehydrogenase complex subunit D | O14521 |
C0030422 | Extra-Adrenal Paraganglioma | SDHD | 6392 | succinate dehydrogenase complex subunit D | O14521 |
C0025268 | Multiple Endocrine Neoplasia Type 2a | SDHD | 6392 | succinate dehydrogenase complex subunit D | O14521 |
C1855008 | Mitochondrial Complex II Deficiency | SDHD | 6392 | succinate dehydrogenase complex subunit D | O14521 |
C1857276 | Trichohepatoenteric Syndrome | SDHD | 6392 | succinate dehydrogenase complex subunit D | O14521 |
C0206754 | Neuroendocrine Tumors | SDHD | 6392 | succinate dehydrogenase complex subunit D | O14521 |
C4048306 | Multiple endocrine neoplasia Type 2 | SDHD | 6392 | succinate dehydrogenase complex subunit D | O14521 |
C0022593 | Keratosis | SDHD | 6392 | succinate dehydrogenase complex subunit D | O14521 |
C0018784 | Sensorineural Hearing Loss (disorder) | SDHD | 6392 | succinate dehydrogenase complex subunit D | O14521 |
C0011570 | Mental Depression | SDHD | 6392 | succinate dehydrogenase complex subunit D | O14521 |
C0265319 | Fibrous skin tumor of tuberous sclerosis | SDHD | 6392 | succinate dehydrogenase complex subunit D | O14521 |
C0007279 | Carotid Body Paraganglioma | SDHD | 6392 | succinate dehydrogenase complex subunit D | O14521 |
C0020437 | Hypercalcemia | SDHD | 6392 | succinate dehydrogenase complex subunit D | O14521 |
C0027831 | Neurofibromatosis 1 | SDHD | 6392 | succinate dehydrogenase complex subunit D | O14521 |
C0346302 | Growth Hormone-Secreting Pituitary Adenoma | SDHD | 6392 | succinate dehydrogenase complex subunit D | O14521 |
C0009402 | Colorectal Carcinoma | SDHD | 6392 | succinate dehydrogenase complex subunit D | O14521 |
C0041296 | Tuberculosis | SDHD | 6392 | succinate dehydrogenase complex subunit D | O14521 |
C0018418 | Gynecomastia | SDHD | 6392 | succinate dehydrogenase complex subunit D | O14521 |
C0233794 | Memory impairment | SDHD | 6392 | succinate dehydrogenase complex subunit D | O14521 |
GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.
Supported by JST NBDC Grant Number JPMJND2204
Partly supported by NIH Common Fund Grant #1U01GM125267-01
GlyCosmos Portal v4.0.0
Last updated: August 19, 2024