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 16126 - 16150 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID Gene Name UniProt ID ▼
C1846672 MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2I DAG1 1605 dystroglycan 1 Q14118
C0266463 Lissencephaly DAG1 1605 dystroglycan 1 Q14118
C1847759 MUSCULAR DYSTROPHY, CONGENITAL, 1C DAG1 1605 dystroglycan 1 Q14118
C0376358 Malignant neoplasm of prostate DAG1 1605 dystroglycan 1 Q14118
C0026010 Microphthalmos DAG1 1605 dystroglycan 1 Q14118
C0153349 Malignant neoplasm of tongue DAG1 1605 dystroglycan 1 Q14118
C0020255 Hydrocephalus DAG1 1605 dystroglycan 1 Q14118
C0007193 Cardiomyopathy, Dilated DAG1 1605 dystroglycan 1 Q14118
C0006826 Malignant Neoplasms DAG1 1605 dystroglycan 1 Q14118
C0027868 Neuromuscular Diseases DAG1 1605 dystroglycan 1 Q14118
C0027092 Myopia DAG1 1605 dystroglycan 1 Q14118
C0033578 Prostatic Neoplasms DAG1 1605 dystroglycan 1 Q14118
C0033860 Psoriasis DAG1 1605 dystroglycan 1 Q14118
C1834674 BETHLEM MYOPATHY 1 DAG1 1605 dystroglycan 1 Q14118
C0023520 Leukodystrophy DAG1 1605 dystroglycan 1 Q14118
C0346647 Malignant neoplasm of pancreas DAG1 1605 dystroglycan 1 Q14118
C0221056 Adult type dermatomyositis DAG1 1605 dystroglycan 1 Q14118
C0006118 Brain Neoplasms DAG1 1605 dystroglycan 1 Q14118
C0026846 Muscular Atrophy DAG1 1605 dystroglycan 1 Q14118
C0029124 Optic Atrophy DAG1 1605 dystroglycan 1 Q14118
C0020538 Hypertensive disease DAG1 1605 dystroglycan 1 Q14118
C0266483 Pachygyria DAG1 1605 dystroglycan 1 Q14118
C0013264 Muscular Dystrophy, Duchenne DAG1 1605 dystroglycan 1 Q14118
C0028754 Obesity DAG1 1605 dystroglycan 1 Q14118
C0878544 Cardiomyopathies DAG1 1605 dystroglycan 1 Q14118

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Last updated: August 19, 2024