autosomal recessive nonsyndromic deafness 9
autosomal recessive nonsyndromic deafness that is characterized by prelingual onset with usually severe to profound, stable hearing loss and has material basis in mutation in the OTOF gene on chromosome 2p23
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autosomal recessive nonsyndromic deafness 9
Summary
autosomal recessive nonsyndromic deafness 9 is a head and neck disease[1].
Key Facts
- autosomal recessive nonsyndromic deafness 9's instance of is recorded as head and neck disease[2].
- autosomal recessive nonsyndromic deafness 9's instance of is recorded as rare disease[3].
- autosomal recessive nonsyndromic deafness 9's instance of is recorded as class of disease[4].
- autosomal recessive nonsyndromic deafness 9 is a type of autosomal recessive nonsyndromic deafness[5].
- autosomal recessive nonsyndromic deafness 9's genetic association is recorded as OTOF[6].
- autosomal recessive nonsyndromic deafness 9's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110535[7].
- autosomal recessive nonsyndromic deafness 9's exact match is recorded as http://identifiers.org/doid/DOID:0110535[8].
- autosomal recessive nonsyndromic deafness 9's on focus list of Wikimedia project is recorded as WikiProject Medicine[9].