Tietz syndrome

Orpha code: 42665OMIM code: 103500

Definition

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.

Disease data
Classification

Malformation syndrome

Synonyms
Hypopigmentation-deafness syndrome
Zespół hipopigmentacja-głuchota
Hypopigmentation-hearing loss syndrome
ORPHA code
42665
OMIM code
103500
ICD10 code
-
ICD11 code
-

No additional description.

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