autosomal dominant nonsyndromic deafness 2A
autosomal dominant nonsyndromic deafness that is characterized by high frequency progressive hearing loss and has material basis in mutation in the KCNQ4 gene on chromosome 1p34.2
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autosomal dominant nonsyndromic deafness 2A
Summary
autosomal dominant nonsyndromic deafness 2A is a head and neck disease[1].
Key Facts
- autosomal dominant nonsyndromic deafness 2A's instance of is recorded as head and neck disease[2].
- autosomal dominant nonsyndromic deafness 2A's instance of is recorded as rare disease[3].
- autosomal dominant nonsyndromic deafness 2A's instance of is recorded as class of disease[4].
- autosomal dominant nonsyndromic deafness 2A's subclass of is recorded as autosomal dominant nonsyndromic deafness[5].
- autosomal dominant nonsyndromic deafness 2A's MeSH descriptor ID is recorded as C567441[6].
- autosomal dominant nonsyndromic deafness 2A's OMIM ID is recorded as 600101[7].
- autosomal dominant nonsyndromic deafness 2A's Disease Ontology ID is recorded as DOID:0110558[8].
- autosomal dominant nonsyndromic deafness 2A's genetic association is recorded as KCNQ4[9].
- autosomal dominant nonsyndromic deafness 2A's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110558[10].
- autosomal dominant nonsyndromic deafness 2A's exact match is recorded as http://identifiers.org/doid/DOID:0110558[11].
- autosomal dominant nonsyndromic deafness 2A's UMLS CUI is recorded as C2677637[12].
- autosomal dominant nonsyndromic deafness 2A's ICD-10-CM is recorded as H90.3[13].
- autosomal dominant nonsyndromic deafness 2A's on focus list of Wikimedia project is recorded as WikiProject Medicine[14].
- autosomal dominant nonsyndromic deafness 2A's Mondo ID is recorded as MONDO_0010817[15].
- autosomal dominant nonsyndromic deafness 2A's UniProt disease ID is recorded as DI-00832[16].