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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 |
| Disease ID | Disease Name | Gene Symbol | Gene ID | Gene Name | UniProt ID ▲ |
|---|---|---|---|---|---|
| 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 |
| C0023467 | Leukemia, Myelocytic, Acute | NTM | 50863 | neurotrimin | Q9P121 |
| C0006826 | Malignant Neoplasms | CLEC1B | 51266 | C-type lectin domain family 1 member B | Q9P126 |
| C0042769 | Virus Diseases | CLEC1B | 51266 | C-type lectin domain family 1 member B | Q9P126 |
| C0000768 | Congenital Abnormality | CLEC1B | 51266 | C-type lectin domain family 1 member B | Q9P126 |
