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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 |
|---|---|---|---|---|---|
| C0268237 | Cytochrome-c Oxidase Deficiency | OTOA | 146183 | otoancorin | Q7RTW8 |
| C1846647 | DEAFNESS, AUTOSOMAL RECESSIVE (disorder) | OTOA | 146183 | otoancorin | Q7RTW8 |
| C1282975 | von Willebrand Disease, Type 2N | OTOA | 146183 | otoancorin | Q7RTW8 |
| C0018784 | Sensorineural Hearing Loss (disorder) | OTOA | 146183 | otoancorin | Q7RTW8 |
| C0302280 | Adrenogenital Syndrome | OTOA | 146183 | otoancorin | Q7RTW8 |
| C1384666 | hearing impairment | OTOA | 146183 | otoancorin | Q7RTW8 |
| C0452138 | Sensorineural hearing loss, bilateral | OTOA | 146183 | otoancorin | Q7RTW8 |
| C3150275 | COMPLEMENT COMPONENT 2 DEFICIENCY | OTOA | 146183 | otoancorin | Q7RTW8 |
| C0001627 | Congenital adrenal hyperplasia | OTOA | 146183 | otoancorin | Q7RTW8 |
| C0221757 | alpha 1-Antitrypsin Deficiency | OTOA | 146183 | otoancorin | Q7RTW8 |
| C1862941 | Amyotrophic Lateral Sclerosis, Sporadic | OTOG | 340990 | otogelin | Q6ZRI0 |
| C3554163 | DEAFNESS, AUTOSOMAL RECESSIVE 18B | OTOG | 340990 | otogelin | Q6ZRI0 |
| C1384666 | hearing impairment | OTOG | 340990 | otogelin | Q6ZRI0 |
| C0011053 | Deafness | OTOG | 340990 | otogelin | Q6ZRI0 |
| C1862939 | AMYOTROPHIC LATERAL SCLEROSIS 1 | OTOG | 340990 | otogelin | Q6ZRI0 |
| C0004096 | Asthma | OTOG | 340990 | otogelin | Q6ZRI0 |
| C0452138 | Sensorineural hearing loss, bilateral | OTOG | 340990 | otogelin | Q6ZRI0 |
| C0009402 | Colorectal Carcinoma | OVGP1 | 5016 | oviductal glycoprotein 1 | Q12889 |
| C0023067 | Laryngitis | OVGP1 | 5016 | oviductal glycoprotein 1 | Q12889 |
| C0269106 | Endosalpingiosis | OVGP1 | 5016 | oviductal glycoprotein 1 | Q12889 |
| C0410207 | Tubular Aggregate Myopathy | OVGP1 | 5016 | oviductal glycoprotein 1 | Q12889 |
| C1140680 | Malignant neoplasm of ovary | OVGP1 | 5016 | oviductal glycoprotein 1 | Q12889 |
| C0004681 | Bagassosis | OVGP1 | 5016 | oviductal glycoprotein 1 | Q12889 |
| C0027651 | Neoplasms | OVGP1 | 5016 | oviductal glycoprotein 1 | Q12889 |
| C0042164 | Uveitis | OVGP1 | 5016 | oviductal glycoprotein 1 | Q12889 |
