autosomal recessive nonsyndromic deafness 49 (Q28024633)
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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
| Language | Label | Description | Also known as |
|---|---|---|---|
| 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 |
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Statements
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C129024
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