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 14101 - 14125 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID ▲ Gene Name UniProt ID
C0410174 Fukuyama Type Congenital Muscular Dystrophy FKTN 2218 fukutin O75072
C0003466 Anus, Imperforate FKTN 2218 fukutin O75072
C0521694 Atrophic retina FKTN 2218 fukutin O75072
C0265221 Walker-Warburg congenital muscular dystrophy FKTN 2218 fukutin O75072
C0006826 Malignant Neoplasms FKTN 2218 fukutin O75072
C0025362 Mental Retardation FKTN 2218 fukutin O75072
C2751052 MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITHOUT MENTAL RETARDATION), TYPE B, 4 FKTN 2218 fukutin O75072
C1852502 CRANIOMETAPHYSEAL DYSPLASIA, AUTOSOMAL DOMINANT FKTN 2218 fukutin O75072
C4284790 Muscular Dystrophy-Dystroglycanopathy (Congenital with Brain and Eye Anomalies) Type A, 1 FKTN 2218 fukutin O75072
C1306459 Primary malignant neoplasm FKTN 2218 fukutin O75072
C0007193 Cardiomyopathy, Dilated FKTN 2218 fukutin O75072
C3714756 Intellectual Disability FKTN 2218 fukutin O75072
C0086543 Cataract FKTN 2218 fukutin O75072
C0020490 Hyperopia FKTN 2218 fukutin O75072
C1969040 MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2M FKTN 2218 fukutin O75072
C3536714 Renal dysplasia FKTN 2218 fukutin O75072
C0878544 Cardiomyopathies FKTN 2218 fukutin O75072
C0270962 Multi-core congenital myopathy FKTN 2218 fukutin O75072
C0026850 Muscular Dystrophy FKTN 2218 fukutin O75072
C3809221 MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 14 FKTN 2218 fukutin O75072
C0575158 Kyphoscoliosis deformity of spine FKTN 2218 fukutin O75072
C0018802 Congestive heart failure FKTN 2218 fukutin O75072
C2875316 Myotubular (centronuclear) myopathy FKTN 2218 fukutin O75072
C0023787 Lipodystrophy FKTN 2218 fukutin O75072
C0686353 Muscular Dystrophies, Limb-Girdle FKTN 2218 fukutin O75072

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Last updated: August 19, 2024