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 62726 - 62743 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID ▲ Gene Name UniProt ID
C1744558 T-lymphocyte deficiency DGCR2 9993 DiGeorge syndrome critical region gene 2 P98153
C0018553 Hamartoma Syndrome, Multiple DGCR2 9993 DiGeorge syndrome critical region gene 2 P98153
C0011854 Diabetes Mellitus, Insulin-Dependent DGCR2 9993 DiGeorge syndrome critical region gene 2 P98153
C0007867 Cervix Diseases DGCR2 9993 DiGeorge syndrome critical region gene 2 P98153
C3250443 MYOTONIC DYSTROPHY 1 DGCR2 9993 DiGeorge syndrome critical region gene 2 P98153
C1840333 Barakat syndrome DGCR2 9993 DiGeorge syndrome critical region gene 2 P98153
C0029456 Osteoporosis DGCR2 9993 DiGeorge syndrome critical region gene 2 P98153
C1306459 Primary malignant neoplasm DGCR2 9993 DiGeorge syndrome critical region gene 2 P98153
C1510586 Autism Spectrum Disorders DGCR2 9993 DiGeorge syndrome critical region gene 2 P98153
C0008312 Primary biliary cirrhosis DGCR2 9993 DiGeorge syndrome critical region gene 2 P98153
C0031900 Pierre Robin Syndrome DGCR2 9993 DiGeorge syndrome critical region gene 2 P98153
C0031511 Pheochromocytoma DGCR2 9993 DiGeorge syndrome critical region gene 2 P98153
C0002726 Amyloidosis DGCR2 9993 DiGeorge syndrome critical region gene 2 P98153
C0158266 Intervertebral Disc Degeneration DGCR2 9993 DiGeorge syndrome critical region gene 2 P98153
C0025958 Microcephaly DGCR2 9993 DiGeorge syndrome critical region gene 2 P98153
C0004364 Autoimmune Diseases DGCR2 9993 DiGeorge syndrome critical region gene 2 P98153
C0005744 Blepharophimosis DGCR2 9993 DiGeorge syndrome critical region gene 2 P98153
C0036572 Seizures DGCR2 9993 DiGeorge syndrome critical region gene 2 P98153

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Last updated: August 19, 2024