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 |
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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Partly supported by NIH Common Fund Grant #1U01GM125267-01
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Last updated: August 19, 2024