autosomal dominant nonsyndromic deafness 10
autosomal dominant nonsyndromic deafness that is characterized by postlingual onset in the third or forth decade of life with a flat or gently downsloping audioprofiles and has material basis in mutation in the EYA4 gene on chromosome 6q23
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autosomal dominant nonsyndromic deafness 10
Summary
autosomal dominant nonsyndromic deafness 10 is a head and neck disease[1].
Key Facts
- autosomal dominant nonsyndromic deafness 10's instance of is recorded as head and neck disease[2].
- autosomal dominant nonsyndromic deafness 10's instance of is recorded as rare disease[3].
- autosomal dominant nonsyndromic deafness 10's instance of is recorded as class of disease[4].
- autosomal dominant nonsyndromic deafness 10's subclass of is recorded as autosomal dominant nonsyndromic deafness[5].
- autosomal dominant nonsyndromic deafness 10's MeSH descriptor ID is recorded as C563354[6].
- autosomal dominant nonsyndromic deafness 10's OMIM ID is recorded as 601316[7].
- autosomal dominant nonsyndromic deafness 10's Disease Ontology ID is recorded as DOID:0110542[8].
- autosomal dominant nonsyndromic deafness 10's NCI Thesaurus ID is recorded as C212887[9].
- autosomal dominant nonsyndromic deafness 10's genetic association is recorded as EYA4[10].
- autosomal dominant nonsyndromic deafness 10's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110542[11].
- autosomal dominant nonsyndromic deafness 10's exact match is recorded as http://identifiers.org/doid/DOID:0110542[12].
- autosomal dominant nonsyndromic deafness 10's UMLS CUI is recorded as C1832476[13].
- autosomal dominant nonsyndromic deafness 10's ICD-10-CM is recorded as H90.3[14].
- autosomal dominant nonsyndromic deafness 10's on focus list of Wikimedia project is recorded as WikiProject Medicine[15].
- autosomal dominant nonsyndromic deafness 10's Mondo ID is recorded as MONDO_0011031[16].
- autosomal dominant nonsyndromic deafness 10's UniProt disease ID is recorded as DI-00840[17].