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 59526 - 59550 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID ▲ Gene Name UniProt ID
C0699790 Colon Carcinoma SMC3 9126 structural maintenance of chromosomes 3 Q9UQE7
C0017574 Gingivitis SMC3 9126 structural maintenance of chromosomes 3 Q9UQE7
C0035334 Retinitis Pigmentosa SMC3 9126 structural maintenance of chromosomes 3 Q9UQE7
C0033770 Prune Belly Syndrome SMC3 9126 structural maintenance of chromosomes 3 Q9UQE7
C0155877 Allergic asthma SMC3 9126 structural maintenance of chromosomes 3 Q9UQE7
C1384666 hearing impairment SMC3 9126 structural maintenance of chromosomes 3 Q9UQE7
C0162429 Malnutrition SMC3 9126 structural maintenance of chromosomes 3 Q9UQE7
C0040021 Thromboangiitis Obliterans SMC3 9126 structural maintenance of chromosomes 3 Q9UQE7
C1956257 Pulmonary Stenosis SMC3 9126 structural maintenance of chromosomes 3 Q9UQE7
C1531647 Cerebral ventriculomegaly SMC3 9126 structural maintenance of chromosomes 3 Q9UQE7
C1855179 CATARACT, ANTERIOR POLAR SMC3 9126 structural maintenance of chromosomes 3 Q9UQE7
C0271007 Phthisis bulbi SMC3 9126 structural maintenance of chromosomes 3 Q9UQE7
C0042580 Vesico-Ureteral Reflux SMC3 9126 structural maintenance of chromosomes 3 Q9UQE7
C0027651 Neoplasms SMC3 9126 structural maintenance of chromosomes 3 Q9UQE7
C0006826 Malignant Neoplasms SMC3 9126 structural maintenance of chromosomes 3 Q9UQE7
C1802395 Congenital muscular hypertrophy-cerebral syndrome SMC3 9126 structural maintenance of chromosomes 3 Q9UQE7
C0266544 Microcornea SMC3 9126 structural maintenance of chromosomes 3 Q9UQE7
C0018784 Sensorineural Hearing Loss (disorder) SMC3 9126 structural maintenance of chromosomes 3 Q9UQE7
C0025160 Megacolon SMC3 9126 structural maintenance of chromosomes 3 Q9UQE7
C0848558 Hypospadias SMC3 9126 structural maintenance of chromosomes 3 Q9UQE7
C0025958 Microcephaly SMC3 9126 structural maintenance of chromosomes 3 Q9UQE7
C0392475 Roberts-SC phocomelia syndrome SMC3 9126 structural maintenance of chromosomes 3 Q9UQE7
C0376358 Malignant neoplasm of prostate SMC3 9126 structural maintenance of chromosomes 3 Q9UQE7
C0221356 Brachycephaly SMC3 9126 structural maintenance of chromosomes 3 Q9UQE7
C0010068 Coronary heart disease SMC3 9126 structural maintenance of chromosomes 3 Q9UQE7

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Last updated: August 19, 2024