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 ...