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 4901 - 4925 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID Gene Name ▼ UniProt ID
C0025958 Microcephaly SMPD4 55627 sphingomyelin phosphodiesterase 4 Q9NXE4
C0027051 Myocardial Infarction SMPD4 55627 sphingomyelin phosphodiesterase 4 Q9NXE4
C0027651 Neoplasms SMPD3 55512 sphingomyelin phosphodiesterase 3 Q9NY59
C0013336 Dwarfism SMPD3 55512 sphingomyelin phosphodiesterase 3 Q9NY59
C2239176 Liver carcinoma SMPD3 55512 sphingomyelin phosphodiesterase 3 Q9NY59
C0006826 Malignant Neoplasms SMPD3 55512 sphingomyelin phosphodiesterase 3 Q9NY59
C0023418 leukemia SMPD3 55512 sphingomyelin phosphodiesterase 3 Q9NY59
C0026918 Mycobacterium Infections SMPD3 55512 sphingomyelin phosphodiesterase 3 Q9NY59
C0003850 Arteriosclerosis SMPD3 55512 sphingomyelin phosphodiesterase 3 Q9NY59
C0020542 Pulmonary Hypertension SMPD3 55512 sphingomyelin phosphodiesterase 3 Q9NY59
C3463824 MYELODYSPLASTIC SYNDROME SMPD3 55512 sphingomyelin phosphodiesterase 3 Q9NY59
C0006142 Malignant neoplasm of breast SMPD3 55512 sphingomyelin phosphodiesterase 3 Q9NY59
C0029434 Osteogenesis Imperfecta SMPD3 55512 sphingomyelin phosphodiesterase 3 Q9NY59
C1561643 Chronic Kidney Diseases SMPD3 55512 sphingomyelin phosphodiesterase 3 Q9NY59
C0268358 Osteogenesis imperfecta, dominant perinatal lethal SMPD3 55512 sphingomyelin phosphodiesterase 3 Q9NY59
C0001342 Acute periodontitis SMPD3 55512 sphingomyelin phosphodiesterase 3 Q9NY59
C0025958 Microcephaly SMPD3 55512 sphingomyelin phosphodiesterase 3 Q9NY59
C0031106 Aggressive Periodontitis SMPD3 55512 sphingomyelin phosphodiesterase 3 Q9NY59
C0024117 Chronic Obstructive Airway Disease SMPD3 55512 sphingomyelin phosphodiesterase 3 Q9NY59
C0268362 Osteogenesis imperfecta type III (disorder) SMPD3 55512 sphingomyelin phosphodiesterase 3 Q9NY59
C1306459 Primary malignant neoplasm SMPD3 55512 sphingomyelin phosphodiesterase 3 Q9NY59
C0242343 Panhypopituitarism SMPD3 55512 sphingomyelin phosphodiesterase 3 Q9NY59
C0027765 nervous system disorder SMPD3 55512 sphingomyelin phosphodiesterase 3 Q9NY59
C2713368 Hematopoetic Myelodysplasia SMPD3 55512 sphingomyelin phosphodiesterase 3 Q9NY59
C1458155 Mammary Neoplasms SMPD3 55512 sphingomyelin phosphodiesterase 3 Q9NY59

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Last updated: August 19, 2024