autosomal recessive nonsyndromic deafness 63
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 LRTOMT gene on chromosome 11q13
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Summary
autosomal recessive nonsyndromic deafness 63 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 63's instance of is recorded as head and neck disease[3].
- autosomal recessive nonsyndromic deafness 63's instance of is recorded as rare disease[4].
- autosomal recessive nonsyndromic deafness 63's instance of is recorded as class of disease[5].
- autosomal recessive nonsyndromic deafness 63 is a type of autosomal recessive nonsyndromic deafness[6].
- autosomal recessive nonsyndromic deafness 63's genetic association is recorded as LRTOMT[7].
- autosomal recessive nonsyndromic deafness 63's genetic association is recorded as TOMT[8].
- autosomal recessive nonsyndromic deafness 63's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110515[9].
- autosomal recessive nonsyndromic deafness 63's exact match is recorded as http://identifiers.org/doid/DOID:0110515[10].
- autosomal recessive nonsyndromic deafness 63's on focus list of Wikimedia project is recorded as WikiProject Medicine[11].
Why It Matters
autosomal recessive nonsyndromic deafness 63 is known by 7 alternative names across languages and contexts.[2]