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 59926 - 59950 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID Gene Name UniProt ID ▼
C0027651 Neoplasms SPTLC2 9517 serine palmitoyltransferase long chain base subunit 2 O15270
C0206664 Teratocarcinoma SPTLC2 9517 serine palmitoyltransferase long chain base subunit 2 O15270
C0027051 Myocardial Infarction SPTLC2 9517 serine palmitoyltransferase long chain base subunit 2 O15270
C0699739 Sensory Neuropathy, Hereditary SPTLC2 9517 serine palmitoyltransferase long chain base subunit 2 O15270
C0011991 Diarrhea SPTLC2 9517 serine palmitoyltransferase long chain base subunit 2 O15270
C0007959 Charcot-Marie-Tooth Disease SPTLC2 9517 serine palmitoyltransferase long chain base subunit 2 O15270
C4721453 Peripheral Nervous System Diseases SPTLC2 9517 serine palmitoyltransferase long chain base subunit 2 O15270
C2239176 Liver carcinoma SPTLC2 9517 serine palmitoyltransferase long chain base subunit 2 O15270
C0003028 Anhidrosis SPTLC2 9517 serine palmitoyltransferase long chain base subunit 2 O15270
C0029443 Osteomyelitis SPTLC2 9517 serine palmitoyltransferase long chain base subunit 2 O15270
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
C0027765 nervous system disorder SPTLC1 10558 serine palmitoyltransferase long chain base subunit 1 O15269
C0031117 Peripheral Neuropathy SPTLC1 10558 serine palmitoyltransferase long chain base subunit 1 O15269
C0442874 Neuropathy SPTLC1 10558 serine palmitoyltransferase long chain base subunit 1 O15269
C4721453 Peripheral Nervous System Diseases SPTLC1 10558 serine palmitoyltransferase long chain base subunit 1 O15269
C0005586 Bipolar Disorder SPTLC1 10558 serine palmitoyltransferase long chain base subunit 1 O15269
C0870082 Hyperkeratosis SPTLC1 10558 serine palmitoyltransferase long chain base subunit 1 O15269
C0027889 Hereditary Sensory and Autonomic Neuropathies SPTLC1 10558 serine palmitoyltransferase long chain base subunit 1 O15269
C0018784 Sensorineural Hearing Loss (disorder) SPTLC1 10558 serine palmitoyltransferase long chain base subunit 1 O15269
C1285162 Degenerative disorder SPTLC1 10558 serine palmitoyltransferase long chain base subunit 1 O15269

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Last updated: August 19, 2024