autosomal recessive nonsyndromic deafness 8
autosomal recessive nonsyndromic deafness that has material basis in mutation in the TMPRSS3 gene on chromosome 21q22
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autosomal recessive nonsyndromic deafness 8
Summary
autosomal recessive nonsyndromic deafness 8 is a head and neck disease[1].
Key Facts
- autosomal recessive nonsyndromic deafness 8's instance of is recorded as head and neck disease[2].
- autosomal recessive nonsyndromic deafness 8's instance of is recorded as rare disease[3].
- autosomal recessive nonsyndromic deafness 8's instance of is recorded as class of disease[4].
- autosomal recessive nonsyndromic deafness 8 is a type of autosomal recessive nonsyndromic deafness[5].
- autosomal recessive nonsyndromic deafness 8's genetic association is recorded as TMPRSS3[6].
- autosomal recessive nonsyndromic deafness 8's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110527[7].
- autosomal recessive nonsyndromic deafness 8's exact match is recorded as http://identifiers.org/doid/DOID:0110527[8].
- autosomal recessive nonsyndromic deafness 8's on focus list of Wikimedia project is recorded as WikiProject Medicine[9].