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Pendred syndrome

Disease Export to PDF
Name:
Pendred syndrome
Description:
A syndromic genetic deafness clinically variable characterized by bilateral sensorineural hearing loss and euthyroid goiter.
ORPHAcode:
705
Synonyms:
Goiter-deafness syndrome
Goiter-hearing loss syndrome
XREF(s):
Orphanet
MeSH
ICD-10
OMIM
Analyte(s):
SLC26A4
KCNJ10
FOXI1
Created:
13 May 2019 - 01:02
Changed:
22 Jun 2023 - 16:14