Term Name: | autosomal recessive nonsyndromic deafness 21 |
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Synonyms: | autosomal recessive deafness 21, DFNB21 |
Definition: | An autosomal recessive nonsyndromic deafness that is characterized by prelingual onset with severe to profound, stable hearing loss and has_material_basis_in mutation in the TECTA gene on chromosome 11q23.3. |
Ontology: | Human Disease [DOID:0110479] ( DOID:0110479 ) |