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 39601 - 39625 of 62743 in total
Disease ID Disease Name Gene Symbol ▲ Gene ID Gene Name UniProt ID
C0026916 Mycobacterium avium-intracellulare Infection NTM 50863 neurotrimin Q9P121
C0238462 Medullary carcinoma of thyroid NTM 50863 neurotrimin Q9P121
C1853230 Aphakia, congenital primary NTM 50863 neurotrimin Q9P121
C0017168 Gastroesophageal reflux disease NTM 50863 neurotrimin Q9P121
C0026918 Mycobacterium Infections NTM 50863 neurotrimin Q9P121
C0024205 Lymphadenitis NTM 50863 neurotrimin Q9P121
C0037274 Dermatologic disorders NTM 50863 neurotrimin Q9P121
C1263846 Attention deficit hyperactivity disorder NTM 50863 neurotrimin Q9P121
C0006267 Bronchiectasis NTM 50863 neurotrimin Q9P121
C0024115 Lung diseases NTM 50863 neurotrimin Q9P121
C0023895 Liver diseases NTM 50863 neurotrimin Q9P121
C2239176 Liver carcinoma NTM 50863 neurotrimin Q9P121
C4551720 Primary Ciliary Dyskinesia NTM 50863 neurotrimin Q9P121
C0024117 Chronic Obstructive Airway Disease NTM 50863 neurotrimin Q9P121
C1836230 HUMAN IMMUNODEFICIENCY VIRUS TYPE 1, SUSCEPTIBILITY TO NTM 50863 neurotrimin Q9P121
C0339573 Glaucoma, Primary Open Angle NTM 50863 neurotrimin Q9P121
C0018798 Congenital Heart Defects NTM 50863 neurotrimin Q9P121
C0037369 Smoking NTM 50863 neurotrimin Q9P121
C1510586 Autism Spectrum Disorders NTM 50863 neurotrimin Q9P121
C0022521 Kartagener Syndrome NTM 50863 neurotrimin Q9P121
C0041696 Unipolar Depression NTM 50863 neurotrimin Q9P121
C0018802 Congestive heart failure NTM 50863 neurotrimin Q9P121
C0027092 Myopia NTM 50863 neurotrimin Q9P121
C1833921 Familial medullary thyroid carcinoma NTM 50863 neurotrimin Q9P121
C0014236 Endophthalmitis NTM 50863 neurotrimin Q9P121

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Last updated: August 19, 2024