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 14826 - 14850 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID ▲ Gene Name UniProt ID
C0015695 Fatty Liver ALDOB 229 aldolase, fructose-bisphosphate B P05062
C0007134 Renal Cell Carcinoma ALDOB 229 aldolase, fructose-bisphosphate B P05062
C0085682 Hypophosphatemia ALDOB 229 aldolase, fructose-bisphosphate B P05062
C0023890 Liver Cirrhosis ALDOB 229 aldolase, fructose-bisphosphate B P05062
C0003467 Anxiety ARSG 22901 arylsulfatase G Q96EG1
C0036341 Schizophrenia ARSG 22901 arylsulfatase G Q96EG1
C0026703 Mucopolysaccharidoses ARSG 22901 arylsulfatase G Q96EG1
C0033578 Prostatic Neoplasms ARSG 22901 arylsulfatase G Q96EG1
C0376358 Malignant neoplasm of prostate ARSG 22901 arylsulfatase G Q96EG1
C1306459 Primary malignant neoplasm ARSG 22901 arylsulfatase G Q96EG1
C0018784 Sensorineural Hearing Loss (disorder) ARSG 22901 arylsulfatase G Q96EG1
C0027877 Neuronal Ceroid-Lipofuscinoses ARSG 22901 arylsulfatase G Q96EG1
C0013421 Dystonia ARSG 22901 arylsulfatase G Q96EG1
C0393593 Dystonia Disorders ARSG 22901 arylsulfatase G Q96EG1
C0154676 Organic writer's cramp ARSG 22901 arylsulfatase G Q96EG1
C1568248 Usher Syndrome, Type III ARSG 22901 arylsulfatase G Q96EG1
C1283601 Deficiency of sulfatase ARSG 22901 arylsulfatase G Q96EG1
C0521694 Atrophic retina ARSG 22901 arylsulfatase G Q96EG1
C0271097 Usher Syndrome ARSG 22901 arylsulfatase G Q96EG1
C0028077 Nyctalopia ARSG 22901 arylsulfatase G Q96EG1
C0007758 Cerebellar Ataxia ARSG 22901 arylsulfatase G Q96EG1
C0743332 Focal Dystonia ARSG 22901 arylsulfatase G Q96EG1
C0004106 Astigmatism ARSG 22901 arylsulfatase G Q96EG1
C0006826 Malignant Neoplasms ARSG 22901 arylsulfatase G Q96EG1
C0005747 Blepharospasm ARSG 22901 arylsulfatase G Q96EG1

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Last updated: August 19, 2024