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 51176 - 51200 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID Gene Name ▲ UniProt ID
C1458155 Mammary Neoplasms PSAP 5660 prosaposin P07602
C0006852 Candidiasis of vagina PSAP 5660 prosaposin P07602
C0008325 Cholecystitis PSAP 5660 prosaposin P07602
C0751279 Metachromatic Leukodystrophy, Adult-Type (disorder) PSAP 5660 prosaposin P07602
C0452138 Sensorineural hearing loss, bilateral PSAP 5660 prosaposin P07602
C0030567 Parkinson Disease PSAP 5660 prosaposin P07602
C1864651 GAUCHER DISEASE, ATYPICAL, DUE TO SAPOSIN C DEFICIENCY PSAP 5660 prosaposin P07602
C2673635 Combined Saposin Deficiency PSAP 5660 prosaposin P07602
C0700345 Candidiasis, Vulvovaginal PSAP 5660 prosaposin P07602
C0751278 Metachromatic Leukodystrophy, Infant PSAP 5660 prosaposin P07602
C0600139 Prostate carcinoma PSAP 5660 prosaposin P07602
C0497327 Dementia PSAP 5660 prosaposin P07602
C0024623 Malignant neoplasm of stomach PSAP 5660 prosaposin P07602
C0027066 Myoclonus PSAP 5660 prosaposin P07602
C0009319 Colitis PSAP 5660 prosaposin P07602
C1621958 Glioblastoma Multiforme PSAP 5660 prosaposin P07602
C0031572 Phobia, Social PSAP 5660 prosaposin P07602
C0011581 Depressive disorder PSAP 5660 prosaposin P07602
C0002871 Anemia PSAP 5660 prosaposin P07602
C0338451 Frontotemporal dementia PSAP 5660 prosaposin P07602
C0040034 Thrombocytopenia PSAP 5660 prosaposin P07602
C0751273 Infantile Globoid Cell Leukodystrophy PSAP 5660 prosaposin P07602
C0520680 Sleep Apnea, Central PSAP 5660 prosaposin P07602
C0002736 Amyotrophic Lateral Sclerosis PSAP 5660 prosaposin P07602
C0006826 Malignant Neoplasms PSAP 5660 prosaposin P07602

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Last updated: August 19, 2024