autosomal dominant nonsyndromic deafness 9
autosomal dominant nonsyndromic deafness that is characterized by postlingual onset in the second decade with high frequency progressive hearing loss and has material basis in mutation in the COCH gene on chromosome 14q12
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autosomal dominant nonsyndromic deafness 9
Summary
autosomal dominant nonsyndromic deafness 9 is a head and neck disease[1].
Key Facts
- autosomal dominant nonsyndromic deafness 9's instance of is recorded as head and neck disease[2].
- autosomal dominant nonsyndromic deafness 9's instance of is recorded as rare disease[3].
- autosomal dominant nonsyndromic deafness 9's instance of is recorded as class of disease[4].
- autosomal dominant nonsyndromic deafness 9's subclass of is recorded as autosomal dominant nonsyndromic deafness[5].
- autosomal dominant nonsyndromic deafness 9's MeSH descriptor ID is recorded as C563335[6].
- autosomal dominant nonsyndromic deafness 9's OMIM ID is recorded as 601369[7].
- autosomal dominant nonsyndromic deafness 9's Disease Ontology ID is recorded as DOID:0110593[8].
- autosomal dominant nonsyndromic deafness 9's genetic association is recorded as COCH[9].
- autosomal dominant nonsyndromic deafness 9's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110593[10].
- autosomal dominant nonsyndromic deafness 9's exact match is recorded as http://identifiers.org/doid/DOID:0110593[11].
- autosomal dominant nonsyndromic deafness 9's UMLS CUI is recorded as C1832425[12].
- autosomal dominant nonsyndromic deafness 9's ICD-10-CM is recorded as H90.3[13].
- autosomal dominant nonsyndromic deafness 9's on focus list of Wikimedia project is recorded as WikiProject Medicine[14].
- autosomal dominant nonsyndromic deafness 9's Mondo ID is recorded as MONDO_0011058[15].
- autosomal dominant nonsyndromic deafness 9's UniProt disease ID is recorded as DI-00839[16].