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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

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Disease ID	Disease Name	Gene Symbol ▼	Gene ID	Gene Name	UniProt ID
C0036341	Schizophrenia	DGCR2	9993	DiGeorge syndrome critical region gene 2	P98153
C0700095	Central neuroblastoma	DGCR2	9993	DiGeorge syndrome critical region gene 2	P98153
C0795907	CONOTRUNCAL ANOMALY FACE SYNDROME	DGCR2	9993	DiGeorge syndrome critical region gene 2	P98153
C3714756	Intellectual Disability	DGCR2	9993	DiGeorge syndrome critical region gene 2	P98153
C0011849	Diabetes Mellitus	DGCR2	9993	DiGeorge syndrome critical region gene 2	P98153
C0012236	DiGeorge Syndrome	DGCR2	9993	DiGeorge syndrome critical region gene 2	P98153
C0018818	Ventricular Septal Defects	DGCR2	9993	DiGeorge syndrome critical region gene 2	P98153
C0018798	Congenital Heart Defects	DGCR2	9993	DiGeorge syndrome critical region gene 2	P98153
C0033770	Prune Belly Syndrome	DGCR2	9993	DiGeorge syndrome critical region gene 2	P98153
C1321551	Shprintzen-Goldberg syndrome	DGCR2	9993	DiGeorge syndrome critical region gene 2	P98153
C0027819	Neuroblastoma	DGCR2	9993	DiGeorge syndrome critical region gene 2	P98153
C0027651	Neoplasms	DGCR2	9993	DiGeorge syndrome critical region gene 2	P98153
C0220704	Shprintzen syndrome	DGCR2	9993	DiGeorge syndrome critical region gene 2	P98153
C1456784	Paranoia	DGCR2	9993	DiGeorge syndrome critical region gene 2	P98153
C1720830	Painful Bladder Syndrome	DGCR2	9993	DiGeorge syndrome critical region gene 2	P98153
C0020626	Hypoparathyroidism	DGCR2	9993	DiGeorge syndrome critical region gene 2	P98153
C0001206	Acromegaly	DGCR2	9993	DiGeorge syndrome critical region gene 2	P98153
C0006826	Malignant Neoplasms	DGCR2	9993	DiGeorge syndrome critical region gene 2	P98153
C0027051	Myocardial Infarction	DGCR2	9993	DiGeorge syndrome critical region gene 2	P98153
C0005586	Bipolar Disorder	DGCR2	9993	DiGeorge syndrome critical region gene 2	P98153
C0011847	Diabetes	DGCR2	9993	DiGeorge syndrome critical region gene 2	P98153
C0013336	Dwarfism	DGCR2	9993	DiGeorge syndrome critical region gene 2	P98153
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

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