autosomal dominant nonsyndromic deafness 4A
autosomal dominant nonsyndromic deafness that is characterized by postlingual onset with flat or gently sloping hearing audioprofiles and has material basis in mutation in the MYH14 gene on chromosome 19q13.33
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autosomal dominant nonsyndromic deafness 4A
Summary
autosomal dominant nonsyndromic deafness 4A is a head and neck disease[1].
Key Facts
- autosomal dominant nonsyndromic deafness 4A's instance of is recorded as head and neck disease[2].
- autosomal dominant nonsyndromic deafness 4A's instance of is recorded as rare disease[3].
- autosomal dominant nonsyndromic deafness 4A's instance of is recorded as class of disease[4].
- autosomal dominant nonsyndromic deafness 4A's subclass of is recorded as autosomal dominant nonsyndromic deafness[5].
- autosomal dominant nonsyndromic deafness 4A's MeSH descriptor ID is recorded as C563460[6].
- autosomal dominant nonsyndromic deafness 4A's OMIM ID is recorded as 600652[7].
- autosomal dominant nonsyndromic deafness 4A's Disease Ontology ID is recorded as DOID:0110573[8].
- autosomal dominant nonsyndromic deafness 4A's genetic association is recorded as MYH14[9].
- autosomal dominant nonsyndromic deafness 4A's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110573[10].
- autosomal dominant nonsyndromic deafness 4A's exact match is recorded as http://identifiers.org/doid/DOID:0110573[11].
- autosomal dominant nonsyndromic deafness 4A's UMLS CUI is recorded as C1833503[12].
- autosomal dominant nonsyndromic deafness 4A's ICD-10-CM is recorded as H90.3[13].
- autosomal dominant nonsyndromic deafness 4A's on focus list of Wikimedia project is recorded as WikiProject Medicine[14].
- autosomal dominant nonsyndromic deafness 4A's Mondo ID is recorded as MONDO_0010915[15].
- autosomal dominant nonsyndromic deafness 4A's UniProt disease ID is recorded as DI-00836[16].