DISEASES

Disease-gene associations mined from literature

Human genes for Pendred Syndrome

Pendred Syndrome [DOID:0060744]

A syndrome characterized by bilateral prelingual sensorineural hearing loss and euthyroid goiter and that has_material_basis_in homozygous or compound heterozygous mutation in the SLC26A4 gene on chromosome 7q.

Synonyms:  Pendred Syndrome,  DOID:0060744,  Pendred disease,  Pendred disorder,  Pendred Syndromes ...