autosomal recessive nonsyndromic deafness 31
autosomal recessive nonsyndromic deafness that is characterized by prelingual onset and has material basis in mutation in the WHRN gene on chromosome 9q32
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autosomal recessive nonsyndromic deafness 31
Summary
autosomal recessive nonsyndromic deafness 31 is a head and neck disease[1].
Key Facts
- autosomal recessive nonsyndromic deafness 31's instance of is recorded as head and neck disease[2].
- autosomal recessive nonsyndromic deafness 31's instance of is recorded as rare disease[3].
- autosomal recessive nonsyndromic deafness 31's instance of is recorded as class of disease[4].
- autosomal recessive nonsyndromic deafness 31 is a type of autosomal recessive nonsyndromic deafness[5].
- autosomal recessive nonsyndromic deafness 31's genetic association is recorded as WHRN[6].
- autosomal recessive nonsyndromic deafness 31's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110490[7].
- autosomal recessive nonsyndromic deafness 31's exact match is recorded as http://identifiers.org/doid/DOID:0110490[8].
- autosomal recessive nonsyndromic deafness 31's on focus list of Wikimedia project is recorded as WikiProject Medicine[9].