autosomal dominant nonsyndromic deafness 11
autosomal dominant nonsyndromic deafness that is characterized by postlingual onset in the first decade of life with a flat or gently downsloping audioprofiles and has material basis in mutation in the MYO7A gene on chromosome 11q13
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autosomal dominant nonsyndromic deafness 11
Summary
autosomal dominant nonsyndromic deafness 11 is a rare disease[1].
Key Facts
- autosomal dominant nonsyndromic deafness 11's instance of is recorded as rare disease[2].
- autosomal dominant nonsyndromic deafness 11's instance of is recorded as class of disease[3].
- autosomal dominant nonsyndromic deafness 11's subclass of is recorded as autosomal dominant nonsyndromic deafness[4].
- autosomal dominant nonsyndromic deafness 11's MeSH descriptor ID is recorded as C563353[5].
- autosomal dominant nonsyndromic deafness 11's OMIM ID is recorded as 601317[6].
- autosomal dominant nonsyndromic deafness 11's Disease Ontology ID is recorded as DOID:0110543[7].
- autosomal dominant nonsyndromic deafness 11's genetic association is recorded as MYO7A[8].
- autosomal dominant nonsyndromic deafness 11's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110543[9].
- autosomal dominant nonsyndromic deafness 11's exact match is recorded as http://identifiers.org/doid/DOID:0110543[10].
- autosomal dominant nonsyndromic deafness 11's UMLS CUI is recorded as C1832475[11].
- autosomal dominant nonsyndromic deafness 11's ICD-10-CM is recorded as H90.3[12].
- autosomal dominant nonsyndromic deafness 11's on focus list of Wikimedia project is recorded as WikiProject Medicine[13].
- autosomal dominant nonsyndromic deafness 11's Mondo ID is recorded as MONDO_0011032[14].
- autosomal dominant nonsyndromic deafness 11's UniProt disease ID is recorded as DI-00841[15].