autosomal recessive nonsyndromic deafness 39 (Q28024624)

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autosomal recessive nonsyndromic deafness that is characterized by prelingual onset with severe to profound, downsloping hearing loss and has material basis in mutation in the HGF gene on chromosome 7q21
  • DFNB39
  • autosomal recessive deafness 39
  • DEAFNESS, AUTOSOMAL RECESSIVE 39; DFNB39
  • Deafness, Autosomal Recessive type 39
  • autosomal recessive nonsyndromic deafness type 39
  • DEAFNESS, AUTOSOMAL RECESSIVE 39
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Language Label Description Also known as
English
autosomal recessive nonsyndromic deafness 39
autosomal recessive nonsyndromic deafness that is characterized by prelingual onset with severe to profound, downsloping hearing loss and has material basis in mutation in the HGF gene on chromosome 7q21
  • DFNB39
  • autosomal recessive deafness 39
  • DEAFNESS, AUTOSOMAL RECESSIVE 39; DFNB39
  • Deafness, Autosomal Recessive type 39
  • autosomal recessive nonsyndromic deafness type 39
  • DEAFNESS, AUTOSOMAL RECESSIVE 39

Statements

instance of
rare disease
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class of disease
0 references

Identifiers

Mondo ID
MONDO_0012003
0 references
 
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