autosomal dominant nonsyndromic deafness 22
autosomal dominant nonsyndromic deafness that is characterized by postlingual onset with high frequency progressive hearing loss and has material basis in mutation in the MYO6 gene on chromosome 6q14
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autosomal dominant nonsyndromic deafness 22
Summary
autosomal dominant nonsyndromic deafness 22 is a developmental defect during embryogenesis[1].
Key Facts
- autosomal dominant nonsyndromic deafness 22's instance of is recorded as developmental defect during embryogenesis[2].
- autosomal dominant nonsyndromic deafness 22's instance of is recorded as head and neck disease[3].
- autosomal dominant nonsyndromic deafness 22's instance of is recorded as rare disease[4].
- autosomal dominant nonsyndromic deafness 22's instance of is recorded as class of disease[5].
- autosomal dominant nonsyndromic deafness 22 is a type of autosomal dominant nonsyndromic deafness[6].
- autosomal dominant nonsyndromic deafness 22 is a type of syndromic genetic deafness[7].
- autosomal dominant nonsyndromic deafness 22 is a type of syndrome associated with hypertrophic cardiomyopathy[8].
- autosomal dominant nonsyndromic deafness 22 is a type of genetic cardiac rhythm disease[9].
- autosomal dominant nonsyndromic deafness 22's genetic association is recorded as MYO6[10].
- autosomal dominant nonsyndromic deafness 22's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110552[11].
- autosomal dominant nonsyndromic deafness 22's exact match is recorded as http://identifiers.org/doid/DOID:0110552[12].
- autosomal dominant nonsyndromic deafness 22's on focus list of Wikimedia project is recorded as WikiProject Medicine[13].