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 59101 - 59125 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID Gene Name UniProt ID ▼
C0494475 Tonic - clonic seizures SYNJ1 8867 synaptojanin 1 O43426
C0011265 Presenile dementia SYNJ1 8867 synaptojanin 1 O43426
C0027066 Myoclonus SYNJ1 8867 synaptojanin 1 O43426
C0002736 Amyotrophic Lateral Sclerosis SYNJ1 8867 synaptojanin 1 O43426
C0028738 Nystagmus SYNJ1 8867 synaptojanin 1 O43426
C1621958 Glioblastoma Multiforme SYNJ1 8867 synaptojanin 1 O43426
C0017636 Glioblastoma SYNJ1 8867 synaptojanin 1 O43426
C0276496 Familial Alzheimer Disease (FAD) SYNJ1 8867 synaptojanin 1 O43426
C0431399 Familial aplasia of the vermis SYNJ1 8867 synaptojanin 1 O43426
C0684276 Hypsarrhythmia SYNJ1 8867 synaptojanin 1 O43426
C0020608 Hypodontia SYNJ1 8867 synaptojanin 1 O43426
C3665347 Visual Impairment SYNJ1 8867 synaptojanin 1 O43426
C0278878 Adult Glioblastoma SYNJ1 8867 synaptojanin 1 O43426
C0027819 Neuroblastoma SYNJ1 8867 synaptojanin 1 O43426
C0004352 Autistic Disorder SYNJ1 8867 synaptojanin 1 O43426
C0026850 Muscular Dystrophy SYNJ1 8867 synaptojanin 1 O43426
C0035334 Retinitis Pigmentosa SYNJ1 8867 synaptojanin 1 O43426
C0700095 Central neuroblastoma SYNJ1 8867 synaptojanin 1 O43426
C0241005 Creatine phosphokinase serum increased SYNJ1 8867 synaptojanin 1 O43426
C3463992 EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 1 SYNJ1 8867 synaptojanin 1 O43426
C1263846 Attention deficit hyperactivity disorder SYNJ1 8867 synaptojanin 1 O43426
C0029124 Optic Atrophy SYNJ1 8867 synaptojanin 1 O43426
C0699885 Carcinoma of bladder GPAA1 8733 glycosylphosphatidylinositol anchor attachment 1 O43292
C0678222 Breast Carcinoma GPAA1 8733 glycosylphosphatidylinositol anchor attachment 1 O43292
C0003635 Apraxias GPAA1 8733 glycosylphosphatidylinositol anchor attachment 1 O43292

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Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: August 19, 2024