autosomal recessive nonsyndromic deafness 88
autosomal recessive nonsyndromic deafness that has material basis in mutation in the ELMOD3 gene on chromosome 2p11
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Summary
autosomal recessive nonsyndromic deafness 88 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 88's instance of is recorded as head and neck disease[3].
- autosomal recessive nonsyndromic deafness 88's instance of is recorded as rare disease[4].
- autosomal recessive nonsyndromic deafness 88's instance of is recorded as class of disease[5].
- autosomal recessive nonsyndromic deafness 88 is a type of autosomal recessive nonsyndromic deafness[6].
- autosomal recessive nonsyndromic deafness 88's genetic association is recorded as ELMOD3[7].
- autosomal recessive nonsyndromic deafness 88's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110533[8].
- autosomal recessive nonsyndromic deafness 88's exact match is recorded as http://identifiers.org/doid/DOID:0110533[9].
- autosomal recessive nonsyndromic deafness 88's on focus list of Wikimedia project is recorded as WikiProject Medicine[10].
Why It Matters
autosomal recessive nonsyndromic deafness 88 is known by 7 alternative names across languages and contexts.[2]