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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 |
|---|---|---|---|---|---|
| C0010701 | Phyllodes Tumor | SDHB | 6390 | succinate dehydrogenase complex iron sulfur subunit B | P21912 |
| C3888391 | Nonnuclear polymorphic congenital cataract | SDHB | 6390 | succinate dehydrogenase complex iron sulfur subunit B | P21912 |
| C0206754 | Neuroendocrine Tumors | SDHB | 6390 | succinate dehydrogenase complex iron sulfur subunit B | P21912 |
| C0001621 | Adrenal Gland Diseases | SDHB | 6390 | succinate dehydrogenase complex iron sulfur subunit B | P21912 |
| C0086769 | Panic Attacks | SDHB | 6390 | succinate dehydrogenase complex iron sulfur subunit B | P21912 |
| C0017658 | Glomerulonephritis | SDHB | 6390 | succinate dehydrogenase complex iron sulfur subunit B | P21912 |
| C0162292 | External Ophthalmoplegia | SDHB | 6390 | succinate dehydrogenase complex iron sulfur subunit B | P21912 |
| C1832370 | MYOPATHY, MYOFIBRILLAR, DESMIN-RELATED | SDHB | 6390 | succinate dehydrogenase complex iron sulfur subunit B | P21912 |
| C0005684 | Malignant neoplasm of urinary bladder | SDHB | 6390 | succinate dehydrogenase complex iron sulfur subunit B | P21912 |
| C1855081 | MICROCEPHALY, PRIMARY AUTOSOMAL RECESSIVE, 1 | SDHB | 6390 | succinate dehydrogenase complex iron sulfur subunit B | P21912 |
| C0013336 | Dwarfism | SDHB | 6390 | succinate dehydrogenase complex iron sulfur subunit B | P21912 |
| C0206734 | Hemangioblastoma | SDHB | 6390 | succinate dehydrogenase complex iron sulfur subunit B | P21912 |
| C0028738 | Nystagmus | SDHB | 6390 | succinate dehydrogenase complex iron sulfur subunit B | P21912 |
| C1704374 | Carcinoma of Endocrine Gland | SDHB | 6390 | succinate dehydrogenase complex iron sulfur subunit B | P21912 |
| C0162429 | Malnutrition | SDHB | 6390 | succinate dehydrogenase complex iron sulfur subunit B | P21912 |
| C1384666 | hearing impairment | SDHB | 6390 | succinate dehydrogenase complex iron sulfur subunit B | P21912 |
| C0086543 | Cataract | SDHB | 6390 | succinate dehydrogenase complex iron sulfur subunit B | P21912 |
| C4551675 | Keratoderma, Palmoplantar | SDHB | 6390 | succinate dehydrogenase complex iron sulfur subunit B | P21912 |
| C1850599 | Leigh Syndrome due to Mitochondrial Complex IV Deficiency | SDHA | 6389 | succinate dehydrogenase complex flavoprotein subunit A | P31040 |
| C0085584 | Encephalopathies | SDHA | 6389 | succinate dehydrogenase complex flavoprotein subunit A | P31040 |
| C0023520 | Leukodystrophy | SDHA | 6389 | succinate dehydrogenase complex flavoprotein subunit A | P31040 |
| C3150898 | CARDIOMYOPATHY, DILATED, 1GG | SDHA | 6389 | succinate dehydrogenase complex flavoprotein subunit A | P31040 |
| C0238198 | Gastrointestinal Stromal Tumors | SDHA | 6389 | succinate dehydrogenase complex flavoprotein subunit A | P31040 |
| C0023264 | Leigh Disease | SDHA | 6389 | succinate dehydrogenase complex flavoprotein subunit A | P31040 |
| C1855008 | Mitochondrial Complex II Deficiency | SDHA | 6389 | succinate dehydrogenase complex flavoprotein subunit A | P31040 |
