autosomal dominant nonsyndromic deafness 9
autosomal dominant nonsyndromic deafness that is characterized by postlingual onset in the second decade with high frequency progressive hearing loss and has material basis in mutation in the COCH gene on chromosome 14q12
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autosomal dominant nonsyndromic deafness 9
Summary
autosomal dominant nonsyndromic deafness 9 is a head and neck disease[1].
Key Facts
- autosomal dominant nonsyndromic deafness 9's instance of is recorded as head and neck disease[2].
- autosomal dominant nonsyndromic deafness 9's instance of is recorded as rare disease[3].
- autosomal dominant nonsyndromic deafness 9's instance of is recorded as class of disease[4].
- autosomal dominant nonsyndromic deafness 9 is a type of autosomal dominant nonsyndromic deafness[5].
- autosomal dominant nonsyndromic deafness 9's genetic association is recorded as COCH[6].
- autosomal dominant nonsyndromic deafness 9's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110593[7].
- autosomal dominant nonsyndromic deafness 9's exact match is recorded as http://identifiers.org/doid/DOID:0110593[8].
- autosomal dominant nonsyndromic deafness 9's on focus list of Wikimedia project is recorded as WikiProject Medicine[9].