autosomal recessive nonsyndromic deafness 22
autosomal recessive nonsyndromic deafness that is characterized by prelingual onset with severe to profound, stable hearing loss and has material basis in mutation in the OTOA gene on chromosome 16p12
Press Enter · cited answer in seconds
0 sources
autosomal recessive nonsyndromic deafness 22
Summary
autosomal recessive nonsyndromic deafness 22 is a head and neck disease[1].
Key Facts
- autosomal recessive nonsyndromic deafness 22's instance of is recorded as head and neck disease[2].
- autosomal recessive nonsyndromic deafness 22's instance of is recorded as rare disease[3].
- autosomal recessive nonsyndromic deafness 22's instance of is recorded as class of disease[4].
- autosomal recessive nonsyndromic deafness 22 is a type of autosomal recessive nonsyndromic deafness[5].
- autosomal recessive nonsyndromic deafness 22's genetic association is recorded as OTOA[6].
- autosomal recessive nonsyndromic deafness 22's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110480[7].
- autosomal recessive nonsyndromic deafness 22's exact match is recorded as http://identifiers.org/doid/DOID:0110480[8].
- autosomal recessive nonsyndromic deafness 22's on focus list of Wikimedia project is recorded as WikiProject Medicine[9].