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 3051 - 3075 of 62743 in total
Disease ID Disease Name Gene Symbol ▼ Gene ID Gene Name UniProt ID
C0025517 Metabolic Diseases TALDO1 6888 transaldolase 1 P37837
C0043346 Xeroderma Pigmentosum TALDO1 6888 transaldolase 1 P37837
C0239946 Fibrosis, Liver TALDO1 6888 transaldolase 1 P37837
C0011847 Diabetes TALDO1 6888 transaldolase 1 P37837
C0011053 Deafness TALDO1 6888 transaldolase 1 P37837
C0016522 Foramen Ovale, Patent TALDO1 6888 transaldolase 1 P37837
C0002895 Anemia, Sickle Cell TALDO1 6888 transaldolase 1 P37837
C0011849 Diabetes Mellitus TALDO1 6888 transaldolase 1 P37837
C0018818 Ventricular Septal Defects TALDO1 6888 transaldolase 1 P37837
C0268419 Acatalasia TALDO1 6888 transaldolase 1 P37837
C2931868 Catalase deficiency TALDO1 6888 transaldolase 1 P37837
C0006142 Malignant neoplasm of breast SYNJ2 8871 synaptojanin 2 O15056
C0086132 Depressive Symptoms SYNJ2 8871 synaptojanin 2 O15056
C0684249 Carcinoma of lung SYNJ2 8871 synaptojanin 2 O15056
C0699790 Colon Carcinoma SYNJ2 8871 synaptojanin 2 O15056
C0431399 Familial aplasia of the vermis SYNJ2 8871 synaptojanin 2 O15056
C0007102 Malignant tumor of colon SYNJ2 8871 synaptojanin 2 O15056
C0026850 Muscular Dystrophy SYNJ2 8871 synaptojanin 2 O15056
C0002736 Amyotrophic Lateral Sclerosis SYNJ2 8871 synaptojanin 2 O15056
C0278878 Adult Glioblastoma SYNJ2 8871 synaptojanin 2 O15056
C0017636 Glioblastoma SYNJ2 8871 synaptojanin 2 O15056
C0013080 Down Syndrome SYNJ1 8867 synaptojanin 1 O43426
C0005586 Bipolar Disorder SYNJ1 8867 synaptojanin 1 O43426
C3809824 PARKINSON DISEASE 20, EARLY-ONSET SYNJ1 8867 synaptojanin 1 O43426
C0025958 Microcephaly SYNJ1 8867 synaptojanin 1 O43426

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Last updated: August 19, 2024