(Q28024633)
English
autosomal recessive nonsyndromic deafness 49
autosomal recessive nonsyndromic deafness that is characterized by prelingual onset with moderate to profound, stable hearing loss and has material basis in mutation in the MARVELD2 gene on chromosome 5q13
- DFNB49
- autosomal recessive deafness 49
- autosomal recessive nonsyndromic deafness type 49
- DEAFNESS, AUTOSOMAL RECESSIVE 49; DFNB49
- Deafness, Autosomal Recessive type 49
- DEAFNESS, AUTOSOMAL RECESSIVE 49
Statements
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C129024
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Identifiers
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