autosomal recessive nonsyndromic deafness 67
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 LHFPL5 gene on chromosome 6p21
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autosomal recessive nonsyndromic deafness 67
Summary
autosomal recessive nonsyndromic deafness 67 is a head and neck disease[1].
Key Facts
- autosomal recessive nonsyndromic deafness 67's instance of is recorded as head and neck disease[2].
- autosomal recessive nonsyndromic deafness 67's instance of is recorded as rare disease[3].
- autosomal recessive nonsyndromic deafness 67's instance of is recorded as class of disease[4].
- autosomal recessive nonsyndromic deafness 67 is a type of autosomal recessive nonsyndromic deafness[5].
- autosomal recessive nonsyndromic deafness 67's genetic association is recorded as LHFPL5[6].
- autosomal recessive nonsyndromic deafness 67's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110518[7].
- autosomal recessive nonsyndromic deafness 67's exact match is recorded as http://identifiers.org/doid/DOID:0110518[8].
- autosomal recessive nonsyndromic deafness 67's on focus list of Wikimedia project is recorded as WikiProject Medicine[9].