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 55876 - 55900 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID ▲ Gene Name UniProt ID
C0036572 Seizures LMAN2L 81562 lectin, mannose binding 2 like Q9H0V9
C0338831 Manic LMAN2L 81562 lectin, mannose binding 2 like Q9H0V9
C1266043 Sarcomatoid Renal Cell Carcinoma LMAN2L 81562 lectin, mannose binding 2 like Q9H0V9
C0008489 Chorea LMAN2L 81562 lectin, mannose binding 2 like Q9H0V9
C0234533 Generalized seizures LMAN2L 81562 lectin, mannose binding 2 like Q9H0V9
C0005587 Depression, Bipolar LMAN2L 81562 lectin, mannose binding 2 like Q9H0V9
C0006012 Borderline Personality Disorder LMAN2L 81562 lectin, mannose binding 2 like Q9H0V9
C0751495 Seizures, Focal LMAN2L 81562 lectin, mannose binding 2 like Q9H0V9
C0279702 Conventional (Clear Cell) Renal Cell Carcinoma LMAN2L 81562 lectin, mannose binding 2 like Q9H0V9
C0038273 Stereotypic Movement Disorder LMAN2L 81562 lectin, mannose binding 2 like Q9H0V9
C1263846 Attention deficit hyperactivity disorder LMAN2L 81562 lectin, mannose binding 2 like Q9H0V9
C1266042 Chromophobe Renal Cell Carcinoma LMAN2L 81562 lectin, mannose binding 2 like Q9H0V9
C1527366 Salaam Seizures LMAN2L 81562 lectin, mannose binding 2 like Q9H0V9
C0013384 Dyskinetic syndrome LMAN2L 81562 lectin, mannose binding 2 like Q9H0V9
C0025958 Microcephaly LMAN2L 81562 lectin, mannose binding 2 like Q9H0V9
C0007134 Renal Cell Carcinoma LMAN2L 81562 lectin, mannose binding 2 like Q9H0V9
C0684276 Hypsarrhythmia LMAN2L 81562 lectin, mannose binding 2 like Q9H0V9
C0235946 Cerebral atrophy LMAN2L 81562 lectin, mannose binding 2 like Q9H0V9
C1306837 Papillary Renal Cell Carcinoma LMAN2L 81562 lectin, mannose binding 2 like Q9H0V9
C0036341 Schizophrenia PLA2G12A 81579 phospholipase A2 group XIIA Q9BZM1
C1510586 Autism Spectrum Disorders PLA2G12A 81579 phospholipase A2 group XIIA Q9BZM1
C0003850 Arteriosclerosis PLA2G12A 81579 phospholipase A2 group XIIA Q9BZM1
C0271084 Exudative age-related macular degeneration PLA2G12A 81579 phospholipase A2 group XIIA Q9BZM1
C0242383 Age related macular degeneration PLA2G12A 81579 phospholipase A2 group XIIA Q9BZM1
C0041296 Tuberculosis ACSBG2 81616 acyl-CoA synthetase bubblegum family member 2 Q5FVE4

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