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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 ▲ |
|---|---|---|---|---|---|
| C0009319 | Colitis | CNTN3 | 5067 | contactin 3 | Q9P232 |
| C0033860 | Psoriasis | CNTN3 | 5067 | contactin 3 | Q9P232 |
| C0003467 | Anxiety | CNTN3 | 5067 | contactin 3 | Q9P232 |
| C0027651 | Neoplasms | CNTN3 | 5067 | contactin 3 | Q9P232 |
| C1282916 | Secondary Raynaud's phenomenon | CNTN3 | 5067 | contactin 3 | Q9P232 |
| C1631597 | VENTRICULAR TACHYCARDIA, CATECHOLAMINERGIC POLYMORPHIC, 1 (disorder) | CNTN3 | 5067 | contactin 3 | Q9P232 |
| C0344315 | Depressed mood | CNTN3 | 5067 | contactin 3 | Q9P232 |
| C0033375 | Prolactinoma | CNTN3 | 5067 | contactin 3 | Q9P232 |
| C0004153 | Atherosclerosis | CNTN3 | 5067 | contactin 3 | Q9P232 |
| C1306459 | Primary malignant neoplasm | CNTN3 | 5067 | contactin 3 | Q9P232 |
| C0022658 | Kidney Diseases | CNTN3 | 5067 | contactin 3 | Q9P232 |
| C0221406 | Pituitary-dependent Cushing's disease | CNTN3 | 5067 | contactin 3 | Q9P232 |
| C1269683 | Major Depressive Disorder | CNTN3 | 5067 | contactin 3 | Q9P232 |
| C0003850 | Arteriosclerosis | CNTN3 | 5067 | contactin 3 | Q9P232 |
| C0013238 | Dry Eye Syndromes | CNTN3 | 5067 | contactin 3 | Q9P232 |
| C0221166 | Paraparesis | CNTN3 | 5067 | contactin 3 | Q9P232 |
| C0086132 | Depressive Symptoms | CNTN3 | 5067 | contactin 3 | Q9P232 |
| C0011991 | Diarrhea | CNTN3 | 5067 | contactin 3 | Q9P232 |
| C0003469 | Anxiety Disorders | CNTN3 | 5067 | contactin 3 | Q9P232 |
| C0022661 | Kidney Failure, Chronic | CNTN3 | 5067 | contactin 3 | Q9P232 |
| C0023976 | Long QT Syndrome | CNTN3 | 5067 | contactin 3 | Q9P232 |
| C0028754 | Obesity | CNTN3 | 5067 | contactin 3 | Q9P232 |
| C0162820 | Dermatitis, Allergic Contact | CNTN3 | 5067 | contactin 3 | Q9P232 |
| C0007194 | Hypertrophic Cardiomyopathy | CNTN3 | 5067 | contactin 3 | Q9P232 |
| C0340427 | Familial dilated cardiomyopathy | CNTN3 | 5067 | contactin 3 | Q9P232 |
