autosomal dominant nonsyndromic deafness 23
autosomal dominant nonsyndromic deafness that is characterized by prelingual onset with high frequency progressive hearing loss and has material basis in mutation in the SIX1 gene on chromosome 14q23
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autosomal dominant nonsyndromic deafness 23
Summary
autosomal dominant nonsyndromic deafness 23 is a head and neck disease[1].
Key Facts
- autosomal dominant nonsyndromic deafness 23's instance of is recorded as head and neck disease[2].
- autosomal dominant nonsyndromic deafness 23's instance of is recorded as rare disease[3].
- autosomal dominant nonsyndromic deafness 23's instance of is recorded as class of disease[4].
- autosomal dominant nonsyndromic deafness 23 is a type of autosomal dominant nonsyndromic deafness[5].
- autosomal dominant nonsyndromic deafness 23's genetic association is recorded as SIX1[6].
- autosomal dominant nonsyndromic deafness 23's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110553[7].
- autosomal dominant nonsyndromic deafness 23's exact match is recorded as http://identifiers.org/doid/DOID:0110553[8].
- autosomal dominant nonsyndromic deafness 23's on focus list of Wikimedia project is recorded as WikiProject Medicine[9].