autosomal recessive nonsyndromic deafness 12
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 CDH23 gene on chromosome 10q22
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autosomal recessive nonsyndromic deafness 12
Summary
autosomal recessive nonsyndromic deafness 12 is a head and neck disease[1].
Key Facts
- autosomal recessive nonsyndromic deafness 12's instance of is recorded as head and neck disease[2].
- autosomal recessive nonsyndromic deafness 12's instance of is recorded as rare disease[3].
- autosomal recessive nonsyndromic deafness 12's instance of is recorded as class of disease[4].
- autosomal recessive nonsyndromic deafness 12 is a type of autosomal recessive nonsyndromic deafness[5].
- autosomal recessive nonsyndromic deafness 12's NCI Thesaurus ID is recorded as C201586[6].
- autosomal recessive nonsyndromic deafness 12's genetic association is recorded as CDH23[7].
- autosomal recessive nonsyndromic deafness 12's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110467[8].
- autosomal recessive nonsyndromic deafness 12's exact match is recorded as http://identifiers.org/doid/DOID:0110467[9].
- autosomal recessive nonsyndromic deafness 12's on focus list of Wikimedia project is recorded as WikiProject Medicine[10].