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 |
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DisGeNET | July 29, 2024 |
Disease ID | Disease Name | Gene Symbol ▼ | Gene ID | Gene Name | UniProt ID |
---|---|---|---|---|---|
C0206698 | Cholangiocarcinoma | ALDOA | 226 | aldolase, fructose-bisphosphate A | P04075 |
C0151744 | Myocardial Ischemia | ALDOA | 226 | aldolase, fructose-bisphosphate A | P04075 |
C1306459 | Primary malignant neoplasm | ALDH9A1 | 223 | aldehyde dehydrogenase 9 family member A1 | P49189 |
C0279702 | Conventional (Clear Cell) Renal Cell Carcinoma | ALDH9A1 | 223 | aldehyde dehydrogenase 9 family member A1 | P49189 |
C0740457 | Malignant neoplasm of kidney | ALDH9A1 | 223 | aldehyde dehydrogenase 9 family member A1 | P49189 |
C0002878 | Anemia, Hemolytic | ALDH9A1 | 223 | aldehyde dehydrogenase 9 family member A1 | P49189 |
C0007134 | Renal Cell Carcinoma | ALDH9A1 | 223 | aldehyde dehydrogenase 9 family member A1 | P49189 |
C0006826 | Malignant Neoplasms | ALDH9A1 | 223 | aldehyde dehydrogenase 9 family member A1 | P49189 |
C0699790 | Colon Carcinoma | ALDH7A1 | 501 | aldehyde dehydrogenase 7 family member A1 | P49419 |
C0036341 | Schizophrenia | ALDH7A1 | 501 | aldehyde dehydrogenase 7 family member A1 | P49419 |
C0006142 | Malignant neoplasm of breast | ALDH7A1 | 501 | aldehyde dehydrogenase 7 family member A1 | P49419 |
C1271398 | Pigment dispersion syndrome (disorder) | ALDH7A1 | 501 | aldehyde dehydrogenase 7 family member A1 | P49419 |
C1704436 | Peripheral Arterial Diseases | ALDH7A1 | 501 | aldehyde dehydrogenase 7 family member A1 | P49419 |
C0751122 | Infantile Severe Myoclonic Epilepsy | ALDH7A1 | 501 | aldehyde dehydrogenase 7 family member A1 | P49419 |
C0023434 | Chronic Lymphocytic Leukemia | ALDH7A1 | 501 | aldehyde dehydrogenase 7 family member A1 | P49419 |
C0242350 | Erectile dysfunction | ALDH7A1 | 501 | aldehyde dehydrogenase 7 family member A1 | P49419 |
C0013595 | Eczema | ALDH7A1 | 501 | aldehyde dehydrogenase 7 family member A1 | P49419 |
C4554007 | Uveoretinal Coloboma | ALDH7A1 | 501 | aldehyde dehydrogenase 7 family member A1 | P49419 |
C0036572 | Seizures | ALDH7A1 | 501 | aldehyde dehydrogenase 7 family member A1 | P49419 |
C0014544 | Epilepsy | ALDH7A1 | 501 | aldehyde dehydrogenase 7 family member A1 | P49419 |
C0029456 | Osteoporosis | ALDH7A1 | 501 | aldehyde dehydrogenase 7 family member A1 | P49419 |
C1839333 | EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 2 | ALDH7A1 | 501 | aldehyde dehydrogenase 7 family member A1 | P49419 |
C3203102 | Idiopathic pulmonary arterial hypertension | ALDH7A1 | 501 | aldehyde dehydrogenase 7 family member A1 | P49419 |
C0549622 | Sexual Dysfunction | ALDH7A1 | 501 | aldehyde dehydrogenase 7 family member A1 | P49419 |
C0015930 | Fetal Distress | ALDH7A1 | 501 | aldehyde dehydrogenase 7 family member A1 | P49419 |
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Last updated: August 19, 2024