autosomal dominant nonsyndromic deafness 15
autosomal dominant nonsyndromic deafness that is characterized by postlingual onset with high frequency progressive hearing loss and has material basis in mutation in the POU4F3 gene on chromosome 5q32
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autosomal dominant nonsyndromic deafness 15
Summary
autosomal dominant nonsyndromic deafness 15 is a head and neck disease[1].
Key Facts
- autosomal dominant nonsyndromic deafness 15's instance of is recorded as head and neck disease[2].
- autosomal dominant nonsyndromic deafness 15's instance of is recorded as rare disease[3].
- autosomal dominant nonsyndromic deafness 15's instance of is recorded as class of disease[4].
- autosomal dominant nonsyndromic deafness 15's subclass of is recorded as autosomal dominant nonsyndromic deafness[5].
- autosomal dominant nonsyndromic deafness 15's MeSH descriptor ID is recorded as C566545[6].
- autosomal dominant nonsyndromic deafness 15's OMIM ID is recorded as 602459[7].
- autosomal dominant nonsyndromic deafness 15's Disease Ontology ID is recorded as DOID:0110546[8].
- autosomal dominant nonsyndromic deafness 15's genetic association is recorded as POU4F3[9].
- autosomal dominant nonsyndromic deafness 15's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110546[10].
- autosomal dominant nonsyndromic deafness 15's exact match is recorded as http://identifiers.org/doid/DOID:0110546[11].
- autosomal dominant nonsyndromic deafness 15's UMLS CUI is recorded as C1865366[12].
- autosomal dominant nonsyndromic deafness 15's ICD-10-CM is recorded as H90.3[13].
- autosomal dominant nonsyndromic deafness 15's on focus list of Wikimedia project is recorded as WikiProject Medicine[14].
- autosomal dominant nonsyndromic deafness 15's Mondo ID is recorded as MONDO_0011226[15].
- autosomal dominant nonsyndromic deafness 15's UniProt disease ID is recorded as DI-00844[16].