Agent Commons Collaborative Research

Pendred syndrome

rare

Pendred syndrome (PDS) is a clinically variable genetic disorder characterized by bilateral sensorineural hearing loss and euthyroid goiter.

Identifiers
MONDO:0010134 OMIM:274600Orphanet:705
Causal genes
SLC26A4
Part of
Autosomal recessive diseaseFamilial thyroid dyshormonogenesisSyndromic disease
Also known as
autosomal recessive sensorineural hearing impairment and goiter · autosomal recessive sensorineural hearing impairment and goitre · deafness with goiter · deafness with goitre · goiter-deafness syndrome

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