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 8626 - 8650 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID ▼ Gene Name UniProt ID
C0005586 Bipolar Disorder POGLUT2 79070 protein O-glucosyltransferase 2 Q6UW63
C4317295 Congenital disorder of glycosylation type 1s ALG8 79053 ALG8 alpha-1,3-glucosyltransferase Q9BVK2
C0011991 Diarrhea ALG8 79053 ALG8 alpha-1,3-glucosyltransferase Q9BVK2
C0015934 Fetal Growth Retardation ALG8 79053 ALG8 alpha-1,3-glucosyltransferase Q9BVK2
C2931002 Congenital disorder of glycosylation type 1H ALG8 79053 ALG8 alpha-1,3-glucosyltransferase Q9BVK2
C0282577 Congenital Disorders of Glycosylation ALG8 79053 ALG8 alpha-1,3-glucosyltransferase Q9BVK2
C0010417 Cryptorchidism ALG8 79053 ALG8 alpha-1,3-glucosyltransferase Q9BVK2
C0079924 Oligohydramnios ALG8 79053 ALG8 alpha-1,3-glucosyltransferase Q9BVK2
C0015930 Fetal Distress ALG8 79053 ALG8 alpha-1,3-glucosyltransferase Q9BVK2
C0020224 Polyhydramnios ALG8 79053 ALG8 alpha-1,3-glucosyltransferase Q9BVK2
C0020676 Hypothyroidism ALG8 79053 ALG8 alpha-1,3-glucosyltransferase Q9BVK2
C3887499 Renal cyst ALG8 79053 ALG8 alpha-1,3-glucosyltransferase Q9BVK2
C0040034 Thrombocytopenia ALG8 79053 ALG8 alpha-1,3-glucosyltransferase Q9BVK2
C0158683 Polycystic liver disease ALG8 79053 ALG8 alpha-1,3-glucosyltransferase Q9BVK2
C0002871 Anemia ALG8 79053 ALG8 alpha-1,3-glucosyltransferase Q9BVK2
C0021831 Intestinal Diseases ALG8 79053 ALG8 alpha-1,3-glucosyltransferase Q9BVK2
C0013274 Patent ductus arteriosus ALG8 79053 ALG8 alpha-1,3-glucosyltransferase Q9BVK2
C0033680 Protein-Losing Enteropathies ALG8 79053 ALG8 alpha-1,3-glucosyltransferase Q9BVK2
C0008370 Cholestasis ALG8 79053 ALG8 alpha-1,3-glucosyltransferase Q9BVK2
C1691228 Cystic Kidney Diseases ALG8 79053 ALG8 alpha-1,3-glucosyltransferase Q9BVK2
C0024236 Lymphedema ALG8 79053 ALG8 alpha-1,3-glucosyltransferase Q9BVK2
C0011581 Depressive disorder ALG8 79053 ALG8 alpha-1,3-glucosyltransferase Q9BVK2
C0009081 Congenital clubfoot ALG8 79053 ALG8 alpha-1,3-glucosyltransferase Q9BVK2
C0018816 Heart Septal Defects ALG8 79053 ALG8 alpha-1,3-glucosyltransferase Q9BVK2
C0086543 Cataract ALG8 79053 ALG8 alpha-1,3-glucosyltransferase Q9BVK2

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Last updated: August 19, 2024