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 2601 - 2625 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID Gene Name ▼ UniProt ID
C0038454 Cerebrovascular accident SFTPA1 653509 surfactant protein A1 Q8IWL2
C0023473 Myeloid Leukemia, Chronic SFTPA1 653509 surfactant protein A1 Q8IWL2
C0751674 Lymphangioleiomyomatosis SFTPA1 653509 surfactant protein A1 Q8IWL2
C0023890 Liver Cirrhosis SFTPA1 653509 surfactant protein A1 Q8IWL2
C0079504 Hermanski-Pudlak Syndrome SFTPA1 653509 surfactant protein A1 Q8IWL2
C0004153 Atherosclerosis SFTPA1 653509 surfactant protein A1 Q8IWL2
C0042769 Virus Diseases SFTPA1 653509 surfactant protein A1 Q8IWL2
C2239176 Liver carcinoma SULT2B1 6820 sulfotransferase family 2B member 1 O00204
C4539754 ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 14 SULT2B1 6820 sulfotransferase family 2B member 1 O00204
C0476089 Endometrial Carcinoma SULT2B1 6820 sulfotransferase family 2B member 1 O00204
C0013336 Dwarfism SULT2B1 6820 sulfotransferase family 2B member 1 O00204
C0870082 Hyperkeratosis SULT2B1 6820 sulfotransferase family 2B member 1 O00204
C0008370 Cholestasis SULT2B1 6820 sulfotransferase family 2B member 1 O00204
C4551630 Ichthyosis Congenita I SULT2B1 6820 sulfotransferase family 2B member 1 O00204
C0376358 Malignant neoplasm of prostate SULT2B1 6820 sulfotransferase family 2B member 1 O00204
C3888093 ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 2 SULT2B1 6820 sulfotransferase family 2B member 1 O00204
C0013592 Ectropion SULT2B1 6820 sulfotransferase family 2B member 1 O00204
C0079583 Ichthyosiform Erythroderma, Congenital SULT2B1 6820 sulfotransferase family 2B member 1 O00204
C0153452 Malignant neoplasm of gallbladder SULT2B1 6820 sulfotransferase family 2B member 1 O00204
C0235782 Gallbladder Carcinoma SULT2B1 6820 sulfotransferase family 2B member 1 O00204
C0271441 Chronic otitis media SULT2B1 6820 sulfotransferase family 2B member 1 O00204
C0079154 Congenital Nonbullous Ichthyosiform Erythroderma SULT2B1 6820 sulfotransferase family 2B member 1 O00204
C0041834 Erythema SULT2B1 6820 sulfotransferase family 2B member 1 O00204
C0020678 Hypotrichosis SULT2B1 6820 sulfotransferase family 2B member 1 O00204
C1565489 Renal Insufficiency SULT2B1 6820 sulfotransferase family 2B member 1 O00204

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Last updated: August 19, 2024