Term Name:	Tietz syndrome
Synonyms:	albinism-deafness of Tietz, hypopigmentation/deafness of Tietz, Tietz albinism-deafness syndrome
Definition:	A syndrome that is characterized by congenital profound bilateral sensorineural hearing loss and generalized albino-like hypopigmentation of skin, eyes and hair that has_material_basis_in mutation in the MITF gene on chromosome 3p13.
Ontology:	Human Disease [DOID:0090002]   ( DOID:0090002 )