autosomal dominant nonsyndromic deafness 2B
autosomal dominant nonsyndromic deafness that is characterized postlingual onset in the fourth decade of life with by high frequency progressive hearing loss and has material basis in mutation in the GJB3 gene on chromosome 1p34.3
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Summary
autosomal dominant nonsyndromic deafness 2B is a head and neck disease[1].
Key Facts
- autosomal dominant nonsyndromic deafness 2B's instance of is recorded as head and neck disease[2].
- autosomal dominant nonsyndromic deafness 2B's instance of is recorded as rare disease[3].
- autosomal dominant nonsyndromic deafness 2B's instance of is recorded as class of disease[4].
- autosomal dominant nonsyndromic deafness 2B is a type of autosomal dominant nonsyndromic deafness[5].
- autosomal dominant nonsyndromic deafness 2B's genetic association is recorded as GJB3[6].
- autosomal dominant nonsyndromic deafness 2B's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110559[7].
- autosomal dominant nonsyndromic deafness 2B's exact match is recorded as http://identifiers.org/doid/DOID:0110559[8].
- autosomal dominant nonsyndromic deafness 2B's on focus list of Wikimedia project is recorded as WikiProject Medicine[9].