autosomal dominant nonsyndromic deafness 40
autosomal dominant nonsyndromic deafness that has material basis in mutation in the CRYM gene on chromosome 16p12
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Summary
autosomal dominant nonsyndromic deafness 40 is a head and neck disease[1]. It is known by 7 alternative names across languages and contexts.[2]
Key Facts
- autosomal dominant nonsyndromic deafness 40's instance of is recorded as head and neck disease[3].
- autosomal dominant nonsyndromic deafness 40's instance of is recorded as rare disease[4].
- autosomal dominant nonsyndromic deafness 40's instance of is recorded as class of disease[5].
- autosomal dominant nonsyndromic deafness 40 is a type of autosomal dominant nonsyndromic deafness[6].
- autosomal dominant nonsyndromic deafness 40's genetic association is recorded as CRYM[7].
- autosomal dominant nonsyndromic deafness 40's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110566[8].
- autosomal dominant nonsyndromic deafness 40's exact match is recorded as http://identifiers.org/doid/DOID:0110566[9].
- autosomal dominant nonsyndromic deafness 40's on focus list of Wikimedia project is recorded as WikiProject Medicine[10].
Why It Matters
autosomal dominant nonsyndromic deafness 40 is known by 7 alternative names across languages and contexts.[2]