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
Displaying entries 4226 - 4250 of 62743 in total
Disease ID Disease Name Gene Symbol ▲ Gene ID Gene Name UniProt ID
C0010346 Crohn Disease ALDH5A1 7915 aldehyde dehydrogenase 5 family member A1 P51649
C0036857 Severe intellectual disability ALDH5A1 7915 aldehyde dehydrogenase 5 family member A1 P51649
C0035372 Rett Syndrome ALDH5A1 7915 aldehyde dehydrogenase 5 family member A1 P51649
C0151744 Myocardial Ischemia ALDH6A1 4329 aldehyde dehydrogenase 6 family member A1 Q02252
C0025958 Microcephaly ALDH6A1 4329 aldehyde dehydrogenase 6 family member A1 Q02252
C0086543 Cataract ALDH6A1 4329 aldehyde dehydrogenase 6 family member A1 Q02252
C0013421 Dystonia ALDH6A1 4329 aldehyde dehydrogenase 6 family member A1 Q02252
C0011860 Diabetes Mellitus, Non-Insulin-Dependent ALDH6A1 4329 aldehyde dehydrogenase 6 family member A1 Q02252
C0014544 Epilepsy ALDH6A1 4329 aldehyde dehydrogenase 6 family member A1 Q02252
C0220981 Metabolic acidosis ALDH6A1 4329 aldehyde dehydrogenase 6 family member A1 Q02252
C0279702 Conventional (Clear Cell) Renal Cell Carcinoma ALDH6A1 4329 aldehyde dehydrogenase 6 family member A1 Q02252
C0028754 Obesity ALDH6A1 4329 aldehyde dehydrogenase 6 family member A1 Q02252
C0026010 Microphthalmos ALDH6A1 4329 aldehyde dehydrogenase 6 family member A1 Q02252
C0268583 Methylmalonic acidemia ALDH6A1 4329 aldehyde dehydrogenase 6 family member A1 Q02252
C0002514 Amino Acid Metabolism, Inborn Errors ALDH6A1 4329 aldehyde dehydrogenase 6 family member A1 Q02252
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

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Last updated: August 19, 2024