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 14676 - 14700 of 62743 in total
Disease ID Disease Name Gene Symbol ▲ Gene ID Gene Name UniProt ID
C0085078 Lysosomal Storage Diseases CTNS 1497 cystinosin, lysosomal cystine transporter O60931
C0030567 Parkinson Disease CTNS 1497 cystinosin, lysosomal cystine transporter O60931
C0341703 Adult Fanconi syndrome CTNS 1497 cystinosin, lysosomal cystine transporter O60931
C1565489 Renal Insufficiency CTNS 1497 cystinosin, lysosomal cystine transporter O60931
C0022658 Kidney Diseases CTNS 1497 cystinosin, lysosomal cystine transporter O60931
C2749685 CYSTINOSIS, ATYPICAL NEPHROPATHIC (disorder) CTNS 1497 cystinosin, lysosomal cystine transporter O60931
C0035309 Retinal Diseases CTNS 1497 cystinosin, lysosomal cystine transporter O60931
C0021364 Male infertility CTNS 1497 cystinosin, lysosomal cystine transporter O60931
C0020619 Hypogonadism CTNS 1497 cystinosin, lysosomal cystine transporter O60931
C0020620 Hypohidrosis CTNS 1497 cystinosin, lysosomal cystine transporter O60931
C0020621 Hypokalemia CTNS 1497 cystinosin, lysosomal cystine transporter O60931
C0035579 Rickets CTNS 1497 cystinosin, lysosomal cystine transporter O60931
C0085636 Photophobia CTNS 1497 cystinosin, lysosomal cystine transporter O60931
C0013336 Dwarfism CTNS 1497 cystinosin, lysosomal cystine transporter O60931
C0033687 Proteinuria CTNS 1497 cystinosin, lysosomal cystine transporter O60931
C0005940 Bone Diseases CTNS 1497 cystinosin, lysosomal cystine transporter O60931
C0085682 Hypophosphatemia CTNS 1497 cystinosin, lysosomal cystine transporter O60931
C0025517 Metabolic Diseases CTNS 1497 cystinosin, lysosomal cystine transporter O60931
C0011849 Diabetes Mellitus CTNS 1497 cystinosin, lysosomal cystine transporter O60931
C3537440 Cystinosis, Infantile Nephropathic CTNS 1497 cystinosin, lysosomal cystine transporter O60931
C1857395 De Toni-Debre-Fanconi Syndrome CTNS 1497 cystinosin, lysosomal cystine transporter O60931
C0151721 Testicular hypogonadism CTNS 1497 cystinosin, lysosomal cystine transporter O60931
C0002395 Alzheimer's Disease CTNS 1497 cystinosin, lysosomal cystine transporter O60931
C0035334 Retinitis Pigmentosa CTNS 1497 cystinosin, lysosomal cystine transporter O60931
C0155119 Recurrent erosion of cornea CTNS 1497 cystinosin, lysosomal cystine transporter O60931

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Last updated: August 19, 2024