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 59001 - 59025 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID Gene Name UniProt ID ▼
C0206157 Myopathies, Nemaline B4GAT1 11041 beta-1,4-glucuronyltransferase 1 O43505
C0026850 Muscular Dystrophy B4GAT1 11041 beta-1,4-glucuronyltransferase 1 O43505
C0020255 Hydrocephalus B4GAT1 11041 beta-1,4-glucuronyltransferase 1 O43505
C2751052 MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITHOUT MENTAL RETARDATION), TYPE B, 4 B4GAT1 11041 beta-1,4-glucuronyltransferase 1 O43505
C0017601 Glaucoma B4GAT1 11041 beta-1,4-glucuronyltransferase 1 O43505
C1257931 Mammary Neoplasms, Human B4GAT1 11041 beta-1,4-glucuronyltransferase 1 O43505
C0751951 Central Core Myopathy (disorder) B4GAT1 11041 beta-1,4-glucuronyltransferase 1 O43505
C0010038 Corneal Opacity B4GAT1 11041 beta-1,4-glucuronyltransferase 1 O43505
C0266551 Congenital coloboma of iris B4GAT1 11041 beta-1,4-glucuronyltransferase 1 O43505
C0020295 Hydronephrosis B4GAT1 11041 beta-1,4-glucuronyltransferase 1 O43505
C0270962 Multi-core congenital myopathy B4GAT1 11041 beta-1,4-glucuronyltransferase 1 O43505
C0086543 Cataract B4GAT1 11041 beta-1,4-glucuronyltransferase 1 O43505
C0266544 Microcornea B4GAT1 11041 beta-1,4-glucuronyltransferase 1 O43505
C0410174 Fukuyama Type Congenital Muscular Dystrophy B4GAT1 11041 beta-1,4-glucuronyltransferase 1 O43505
C3809221 MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 14 B4GAT1 11041 beta-1,4-glucuronyltransferase 1 O43505
C0026010 Microphthalmos B4GAT1 11041 beta-1,4-glucuronyltransferase 1 O43505
C0678222 Breast Carcinoma B4GAT1 11041 beta-1,4-glucuronyltransferase 1 O43505
C0010417 Cryptorchidism B4GAT1 11041 beta-1,4-glucuronyltransferase 1 O43505
C0029124 Optic Atrophy B4GAT1 11041 beta-1,4-glucuronyltransferase 1 O43505
C0035305 Retinal Detachment B4GAT1 11041 beta-1,4-glucuronyltransferase 1 O43505
C0025958 Microcephaly B4GAT1 11041 beta-1,4-glucuronyltransferase 1 O43505
C0010964 Dandy-Walker Syndrome B4GAT1 11041 beta-1,4-glucuronyltransferase 1 O43505
C0241005 Creatine phosphokinase serum increased B4GAT1 11041 beta-1,4-glucuronyltransferase 1 O43505
C0020615 Hypoglycemia MGAM 8972 maltase-glucoamylase O43451
C0011860 Diabetes Mellitus, Non-Insulin-Dependent MGAM 8972 maltase-glucoamylase O43451

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Last updated: August 19, 2024