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 2751 - 2775 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID Gene Name UniProt ID ▲
C0043459 Zellweger Syndrome GNPAT 8443 glyceronephosphate O-acyltransferase O15228
C1263846 Attention deficit hyperactivity disorder GNPAT 8443 glyceronephosphate O-acyltransferase O15228
C0008445 Chondrodysplasia Punctata GNPAT 8443 glyceronephosphate O-acyltransferase O15228
C0036341 Schizophrenia GNPAT 8443 glyceronephosphate O-acyltransferase O15228
C0025958 Microcephaly GNPAT 8443 glyceronephosphate O-acyltransferase O15228
C0004352 Autistic Disorder GNPAT 8443 glyceronephosphate O-acyltransferase O15228
C0041671 Attention Deficit Disorder GNPAT 8443 glyceronephosphate O-acyltransferase O15228
C0006826 Malignant Neoplasms GNPAT 8443 glyceronephosphate O-acyltransferase O15228
C0279000 Liver and Intrahepatic Biliary Tract Carcinoma GNPAT 8443 glyceronephosphate O-acyltransferase O15228
C0036439 Scoliosis, unspecified GNPAT 8443 glyceronephosphate O-acyltransferase O15228
C0345904 Malignant neoplasm of liver GNPAT 8443 glyceronephosphate O-acyltransferase O15228
C1306459 Primary malignant neoplasm GNPAT 8443 glyceronephosphate O-acyltransferase O15228
C0086543 Cataract GNPAT 8443 glyceronephosphate O-acyltransferase O15228
C0002395 Alzheimer's Disease GNPAT 8443 glyceronephosphate O-acyltransferase O15228
C2239176 Liver carcinoma GNPAT 8443 glyceronephosphate O-acyltransferase O15228
C0239946 Fibrosis, Liver GNPAT 8443 glyceronephosphate O-acyltransferase O15228
C0600139 Prostate carcinoma ACOX3 8310 acyl-CoA oxidase 3, pristanoyl O15254
C0033578 Prostatic Neoplasms ACOX3 8310 acyl-CoA oxidase 3, pristanoyl O15254
C0376358 Malignant neoplasm of prostate ACOX3 8310 acyl-CoA oxidase 3, pristanoyl O15254
C0004936 Mental disorders SPTLC1 10558 serine palmitoyltransferase long chain base subunit 1 O15269
C0020071 Hereditary Sensory Autonomic Neuropathy, Type 1 SPTLC1 10558 serine palmitoyltransferase long chain base subunit 1 O15269
C0033975 Psychotic Disorders SPTLC1 10558 serine palmitoyltransferase long chain base subunit 1 O15269
C0086405 Hereditary Sensory Radicular Neuropathy SPTLC1 10558 serine palmitoyltransferase long chain base subunit 1 O15269
C0006118 Brain Neoplasms SPTLC1 10558 serine palmitoyltransferase long chain base subunit 1 O15269
C0007959 Charcot-Marie-Tooth Disease SPTLC1 10558 serine palmitoyltransferase long chain base subunit 1 O15269

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Last updated: August 19, 2024