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 7101 - 7125 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID Gene Name ▲ UniProt ID
C1263846 Attention deficit hyperactivity disorder OCRL 4952 OCRL inositol polyphosphate-5-phosphatase Q01968
C0020621 Hypokalemia OCRL 4952 OCRL inositol polyphosphate-5-phosphatase Q01968
C0010038 Corneal Opacity OCRL 4952 OCRL inositol polyphosphate-5-phosphatase Q01968
C0025362 Mental Retardation OCRL 4952 OCRL inositol polyphosphate-5-phosphatase Q01968
C3665347 Visual Impairment OCRL 4952 OCRL inositol polyphosphate-5-phosphatase Q01968
C0011334 Dental caries OCRL 4952 OCRL inositol polyphosphate-5-phosphatase Q01968
C0036572 Seizures OCRL 4952 OCRL inositol polyphosphate-5-phosphatase Q01968
C0029408 Degenerative polyarthritis OCRL 4952 OCRL inositol polyphosphate-5-phosphatase Q01968
C0035078 Kidney Failure OCRL 4952 OCRL inositol polyphosphate-5-phosphatase Q01968
C0024523 Malabsorption Syndrome OCRL 4952 OCRL inositol polyphosphate-5-phosphatase Q01968
C0037299 Skin Ulcer OCRL 4952 OCRL inositol polyphosphate-5-phosphatase Q01968
C0037286 Skin Neoplasms OCRL 4952 OCRL inositol polyphosphate-5-phosphatase Q01968
C0020438 Hypercalciuria OCRL 4952 OCRL inositol polyphosphate-5-phosphatase Q01968
C0241005 Creatine phosphokinase serum increased OCRL 4952 OCRL inositol polyphosphate-5-phosphatase Q01968
C0035579 Rickets OCRL 4952 OCRL inositol polyphosphate-5-phosphatase Q01968
C1848336 Dent disease 1 OCRL 4952 OCRL inositol polyphosphate-5-phosphatase Q01968
C0014761 Erythroblastosis, Fetal OCRL 4952 OCRL inositol polyphosphate-5-phosphatase Q01968
C0010417 Cryptorchidism OCRL 4952 OCRL inositol polyphosphate-5-phosphatase Q01968
C0020428 Hyperaldosteronism OCRL 4952 OCRL inositol polyphosphate-5-phosphatase Q01968
C1848201 Subcortical Band Heterotopia OCRL 4952 OCRL inositol polyphosphate-5-phosphatase Q01968
C1621958 Glioblastoma Multiforme OCRL 4952 OCRL inositol polyphosphate-5-phosphatase Q01968
C0151491 Congenital musculoskeletal anomalies OCRL 4952 OCRL inositol polyphosphate-5-phosphatase Q01968
C0268435 Renal Tubular Acidosis, Type II OCRL 4952 OCRL inositol polyphosphate-5-phosphatase Q01968
C0028738 Nystagmus OCRL 4952 OCRL inositol polyphosphate-5-phosphatase Q01968
C3887650 Adult Rickets OCRL 4952 OCRL inositol polyphosphate-5-phosphatase Q01968

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Last updated: August 19, 2024