autosomal dominant nonsyndromic deafness 4A
autosomal dominant nonsyndromic deafness that is characterized by postlingual onset with flat or gently sloping hearing audioprofiles and has material basis in mutation in the MYH14 gene on chromosome 19q13.33
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autosomal dominant nonsyndromic deafness 4A
Summary
autosomal dominant nonsyndromic deafness 4A is a head and neck disease[1].
Key Facts
- autosomal dominant nonsyndromic deafness 4A's instance of is recorded as head and neck disease[2].
- autosomal dominant nonsyndromic deafness 4A's instance of is recorded as rare disease[3].
- autosomal dominant nonsyndromic deafness 4A's instance of is recorded as class of disease[4].
- autosomal dominant nonsyndromic deafness 4A is a type of autosomal dominant nonsyndromic deafness[5].
- autosomal dominant nonsyndromic deafness 4A's genetic association is recorded as MYH14[6].
- autosomal dominant nonsyndromic deafness 4A's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110573[7].
- autosomal dominant nonsyndromic deafness 4A's exact match is recorded as http://identifiers.org/doid/DOID:0110573[8].
- autosomal dominant nonsyndromic deafness 4A's on focus list of Wikimedia project is recorded as WikiProject Medicine[9].