autosomal dominant nonsyndromic deafness 10
autosomal dominant nonsyndromic deafness that is characterized by postlingual onset in the third or forth decade of life with a flat or gently downsloping audioprofiles and has material basis in mutation in the EYA4 gene on chromosome 6q23
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Summary
autosomal dominant nonsyndromic deafness 10 is a head and neck disease[1].
Key Facts
- autosomal dominant nonsyndromic deafness 10's instance of is recorded as head and neck disease[2].
- autosomal dominant nonsyndromic deafness 10's instance of is recorded as rare disease[3].
- autosomal dominant nonsyndromic deafness 10's instance of is recorded as class of disease[4].
- autosomal dominant nonsyndromic deafness 10 is a type of autosomal dominant nonsyndromic deafness[5].
- autosomal dominant nonsyndromic deafness 10's NCI Thesaurus ID is recorded as C212887[6].
- autosomal dominant nonsyndromic deafness 10's genetic association is recorded as EYA4[7].
- autosomal dominant nonsyndromic deafness 10's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110542[8].
- autosomal dominant nonsyndromic deafness 10's exact match is recorded as http://identifiers.org/doid/DOID:0110542[9].
- autosomal dominant nonsyndromic deafness 10's on focus list of Wikimedia project is recorded as WikiProject Medicine[10].