Human disease
Tietz syndrome
Mondo defines it as: “Tietz syndrome is a genetic hypopigmentation and deafness syndrome characterized by congenital profound bilateral sensorineural hearing loss and generalized albino-like hypopigmentation of skin, eyes and hair.”
3 disease groups in OMIA reach this disease, through OMIA's own Mondo link or its OMIM numbers. The page shows the chain. It does not say whether an animal is a model of this disease.
Animal diseases
By natural-model score for this disease, highest first. The score says how complete and how well supported each chain is, by stated rules. How the score works.
| OMIA group | Name | Found by | Species | The chain reached | Score |
|---|---|---|---|---|---|
| 1680 | Coat colour, dominant white with bilateral deafness | OMIA's OMIM numbers | 2 | Target evidence |
59.0
|
| 214 | Coat colour, white spotting | OMIA's OMIM numbers | 7 | Target evidence |
56.0
|
| 1931 | Depigmentation associated with microphthalmia | OMIA's OMIM numbers | 1 | Target evidence |
56.0
|
Human genes
Each human gene of these disease groups that Open Targets links to this disease.
| Human gene | Score | Evidence |
|---|---|---|
| MITF | 0.77 | 1,135 |
Drugs tested for this disease
Each ChEMBL drug that has been tested for this disease, and the human genes above it acts on, if any. Open Targets gives some drugs, such as most enzyme replacement therapies, no target gene.
No drug has been tested for this disease.