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 1101 - 1125 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID ▼ Gene Name UniProt ID
C0013080 Down Syndrome CD38 952 CD38 molecule P28907
C0023418 leukemia CD38 952 CD38 molecule P28907
C1961102 Precursor Cell Lymphoblastic Leukemia Lymphoma CD38 952 CD38 molecule P28907
C0026764 Multiple Myeloma CD38 952 CD38 molecule P28907
C1868683 B-CELL MALIGNANCY, LOW-GRADE CD38 952 CD38 molecule P28907
C0004352 Autistic Disorder CD38 952 CD38 molecule P28907
C0026769 Multiple Sclerosis CD38 952 CD38 molecule P28907
C3275445 X-linked immunodeficiency with magnesium defect, Epstein-Barr virus infection and neoplasia CD38 952 CD38 molecule P28907
C0009447 Common Variable Immunodeficiency CD38 952 CD38 molecule P28907
C0041296 Tuberculosis CD38 952 CD38 molecule P28907
C1510586 Autism Spectrum Disorders CD38 952 CD38 molecule P28907
C0006826 Malignant Neoplasms CD38 952 CD38 molecule P28907
C1271398 Pigment dispersion syndrome (disorder) CD38 952 CD38 molecule P28907
C4317091 Trisomy 18 Syndrome CD38 952 CD38 molecule P28907
C0152018 Esophageal carcinoma CD38 952 CD38 molecule P28907
C0023467 Leukemia, Myelocytic, Acute CD38 952 CD38 molecule P28907
C0079731 B-Cell Lymphomas CD38 952 CD38 molecule P28907
C3463824 MYELODYSPLASTIC SYNDROME CD38 952 CD38 molecule P28907
C4041080 Neurocognitive Disorders CD38 952 CD38 molecule P28907
C0023473 Myeloid Leukemia, Chronic CD38 952 CD38 molecule P28907
C0027651 Neoplasms CD38 952 CD38 molecule P28907
C0023452 Childhood Acute Lymphoblastic Leukemia CD38 952 CD38 molecule P28907
C0023787 Lipodystrophy CD38 952 CD38 molecule P28907
C0700095 Central neuroblastoma CD38 952 CD38 molecule P28907
C0349631 Richter's syndrome CD38 952 CD38 molecule P28907

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Last updated: August 19, 2024