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 60851 - 60875 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID ▼ Gene Name UniProt ID
C0028738 Nystagmus EBP 10682 EBP cholestenol delta-isomerase Q15125
C0020295 Hydronephrosis EBP 10682 EBP cholestenol delta-isomerase Q15125
C0036341 Schizophrenia EBP 10682 EBP cholestenol delta-isomerase Q15125
C0007134 Renal Cell Carcinoma EBP 10682 EBP cholestenol delta-isomerase Q15125
C0017638 Glioma EBP 10682 EBP cholestenol delta-isomerase Q15125
C3714756 Intellectual Disability EBP 10682 EBP cholestenol delta-isomerase Q15125
C1859126 Stippled epiphyses EBP 10682 EBP cholestenol delta-isomerase Q15125
C0007102 Malignant tumor of colon EBP 10682 EBP cholestenol delta-isomerase Q15125
C0020758 Congenital ichthyosis EBP 10682 EBP cholestenol delta-isomerase Q15125
C0007785 Cerebral Infarction EBP 10682 EBP cholestenol delta-isomerase Q15125
C0022735 Klinefelter Syndrome EBP 10682 EBP cholestenol delta-isomerase Q15125
C0009081 Congenital clubfoot EBP 10682 EBP cholestenol delta-isomerase Q15125
C0019196 Hepatitis C EBP 10682 EBP cholestenol delta-isomerase Q15125
C0020255 Hydrocephalus EBP 10682 EBP cholestenol delta-isomerase Q15125
C0008925 Cleft Palate EBP 10682 EBP cholestenol delta-isomerase Q15125
C0008497 Choriocarcinoma EBP 10682 EBP cholestenol delta-isomerase Q15125
C0023448 Lymphoid leukemia EBP 10682 EBP cholestenol delta-isomerase Q15125
C0699885 Carcinoma of bladder EBP 10682 EBP cholestenol delta-isomerase Q15125
C0018784 Sensorineural Hearing Loss (disorder) EBP 10682 EBP cholestenol delta-isomerase Q15125
C0037274 Dermatologic disorders EBP 10682 EBP cholestenol delta-isomerase Q15125
C0013604 Edema EBP 10682 EBP cholestenol delta-isomerase Q15125
C0018213 Graves Disease B3GNT2 10678 UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 2 Q9NY97
C0265221 Walker-Warburg congenital muscular dystrophy B3GNT2 10678 UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 2 Q9NY97
C0036341 Schizophrenia B3GNT2 10678 UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 2 Q9NY97
C0027651 Neoplasms B3GNT2 10678 UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 2 Q9NY97

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Last updated: August 19, 2024