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 40451 - 40475 of 62743 in total
Disease ID Disease Name Gene Symbol ▼ Gene ID Gene Name UniProt ID
C0344559 Irido-corneo-trabecular dysgenesis (disorder) FKTN 2218 fukutin O75072
C0344530 Congenital keratoglobus FKTN 2218 fukutin O75072
C1836373 MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2K FKTN 2218 fukutin O75072
C0036857 Severe intellectual disability FKTN 2218 fukutin O75072
C0546264 Congenital Fiber Type Disproportion FKTN 2218 fukutin O75072
C0027092 Myopia FKTN 2218 fukutin O75072
C0017601 Glaucoma FKTN 2218 fukutin O75072
C0010964 Dandy-Walker Syndrome FKTN 2218 fukutin O75072
C0038379 Strabismus FKTN 2218 fukutin O75072
C0024623 Malignant neoplasm of stomach FKTN 2218 fukutin O75072
C0015934 Fetal Growth Retardation FKTN 2218 fukutin O75072
C0235782 Gallbladder Carcinoma FKTN 2218 fukutin O75072
C0004114 Astrocytoma FKTN 2218 fukutin O75072
C1531647 Cerebral ventriculomegaly FKTN 2218 fukutin O75072
C0025958 Microcephaly FKTN 2218 fukutin O75072
C0010417 Cryptorchidism FKTN 2218 fukutin O75072
C0266551 Congenital coloboma of iris FKTN 2218 fukutin O75072
C0751951 Central Core Myopathy (disorder) FKTN 2218 fukutin O75072
C1861922 CAMPOMELIC DYSPLASIA FKTN 2218 fukutin O75072
C1261470 Congenital meningocele FKTN 2218 fukutin O75072
C0153452 Malignant neoplasm of gallbladder FKTN 2218 fukutin O75072
C0037822 Speech Disorders FKTN 2218 fukutin O75072
C1956257 Pulmonary Stenosis FKTN 2218 fukutin O75072
C0206157 Myopathies, Nemaline FKTN 2218 fukutin O75072
C3665347 Visual Impairment FKTN 2218 fukutin O75072

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Last updated: August 19, 2024