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Tietz syndrome

Disease Export to PDF
Name:
Tietz syndrome
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.
ORPHAcode:
42665
Synonyms:
Hypopigmentation-deafness syndrome
Hypopigmentation-hearing loss syndrome
XREF(s):
Orphanet
ICD-10
OMIM
MeSH
Analyte(s):
MITF
Created:
13 May 2019 - 01:02
Changed:
22 Jun 2023 - 16:14