(Q28024604)
English
autosomal recessive nonsyndromic deafness 21
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.
- DFNB21
- autosomal recessive deafness 21
- DEAFNESS, AUTOSOMAL RECESSIVE 21; DFNB21
- autosomal recessive nonsyndromic deafness type 21
- Deafness, Autosomal Recessive type 21
- DEAFNESS, AUTOSOMAL RECESSIVE 21
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