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 44026 - 44050 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID ▲ Gene Name UniProt ID
C0015934 Fetal Growth Retardation PRNP 5621 prion protein P04156
C0000768 Congenital Abnormality PRNP 5621 prion protein P04156
C0017636 Glioblastoma PRNP 5621 prion protein P04156
C0041696 Unipolar Depression PRNP 5621 prion protein P04156
C1306459 Primary malignant neoplasm PRNP 5621 prion protein P04156
C0339573 Glaucoma, Primary Open Angle PRNP 5621 prion protein P04156
C0006826 Malignant Neoplasms PRNP 5621 prion protein P04156
C0003635 Apraxias PRNP 5621 prion protein P04156
C0038644 Sudden infant death syndrome PRNP 5621 prion protein P04156
C0021390 Inflammatory Bowel Diseases PRNP 5621 prion protein P04156
C0028754 Obesity PRNP 5621 prion protein P04156
C0152025 Polyneuropathy PRNP 5621 prion protein P04156
C0699791 Stomach Carcinoma PRNP 5621 prion protein P04156
C0026769 Multiple Sclerosis PRNP 5621 prion protein P04156
C0678222 Breast Carcinoma PRNP 5621 prion protein P04156
C0162635 Angelman Syndrome PRNP 5621 prion protein P04156
C0236642 Pick Disease of the Brain PRNP 5621 prion protein P04156
C0039103 Synovitis PRNP 5621 prion protein P04156
C0003537 Aphasia PRNP 5621 prion protein P04156
C0024623 Malignant neoplasm of stomach PRNP 5621 prion protein P04156
C0009404 Colorectal Neoplasms PRNP 5621 prion protein P04156
C1832661 ANOPHTHALMIA AND PULMONARY HYPOPLASIA PRNP 5621 prion protein P04156
C0014544 Epilepsy PRNP 5621 prion protein P04156
C0338451 Frontotemporal dementia PRNP 5621 prion protein P04156
C1853926 NONAKA MYOPATHY PRNP 5621 prion protein P04156

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Last updated: August 19, 2024