autosomal recessive nonsyndromic deafness 61
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 SLC26A5 gene on chromosome 7q22
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Summary
autosomal recessive nonsyndromic deafness 61 is a head and neck disease[1]. It is known by 7 alternative names across languages and contexts.[2]
Key Facts
- autosomal recessive nonsyndromic deafness 61's instance of is recorded as head and neck disease[3].
- autosomal recessive nonsyndromic deafness 61's instance of is recorded as rare disease[4].
- autosomal recessive nonsyndromic deafness 61's instance of is recorded as class of disease[5].
- autosomal recessive nonsyndromic deafness 61 is a type of autosomal recessive nonsyndromic deafness[6].
- autosomal recessive nonsyndromic deafness 61's genetic association is recorded as SLC26A5[7].
- autosomal recessive nonsyndromic deafness 61's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110513[8].
- autosomal recessive nonsyndromic deafness 61's exact match is recorded as http://identifiers.org/doid/DOID:0110513[9].
- autosomal recessive nonsyndromic deafness 61's on focus list of Wikimedia project is recorded as WikiProject Medicine[10].
Why It Matters
autosomal recessive nonsyndromic deafness 61 is known by 7 alternative names across languages and contexts.[2]