Term Name: | autosomal recessive nonsyndromic deafness 29 |
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Synonyms: | autosomal recessive deafness 29, DFNB29 |
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 CLDN14 gene on chromosome 21q22. |
Ontology: | Human Disease [DOID:0110487] ( DOID:0110487 ) |