autosomal recessive nonsyndromic deafness 77
autosomal recessive nonsyndromic deafness that is characterized by postlingual onset with moderate to profound, progressive hearing loss and has material basis in mutation in the LOXHD1 gene on chromosome 18q21
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autosomal recessive nonsyndromic deafness 77
Summary
autosomal recessive nonsyndromic deafness 77 is a head and neck disease[1].
Key Facts
- autosomal recessive nonsyndromic deafness 77's instance of is recorded as head and neck disease[2].
- autosomal recessive nonsyndromic deafness 77's instance of is recorded as rare disease[3].
- autosomal recessive nonsyndromic deafness 77's instance of is recorded as class of disease[4].
- autosomal recessive nonsyndromic deafness 77 is a type of autosomal recessive nonsyndromic deafness[5].
- autosomal recessive nonsyndromic deafness 77's genetic association is recorded as LOXHD1[6].
- autosomal recessive nonsyndromic deafness 77's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110525[7].
- autosomal recessive nonsyndromic deafness 77's exact match is recorded as http://identifiers.org/doid/DOID:0110525[8].
- autosomal recessive nonsyndromic deafness 77's on focus list of Wikimedia project is recorded as WikiProject Medicine[9].