|Dataset||CTD Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||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. (Orphanet Rare Disease Ontology, Orphanet_42665)|
|Downloads & Tools|
1 genes/proteins associated with the disease Tietz syndrome from the curated CTD Gene-Disease Associations dataset.
|MITF||microphthalmia-associated transcription factor||2.88009|