autosomal dominant nonsyndromic deafness 13
autosomal dominant nonsyndromic deafness that is characterized by postlingual onset in the second decade of life with mid-frequency hearing loss and has material basis in mutation in the COL11A2 gene on chromosome 6p21
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autosomal dominant nonsyndromic deafness 13
Summary
autosomal dominant nonsyndromic deafness 13 is a head and neck disease[1].
Key Facts
- autosomal dominant nonsyndromic deafness 13's instance of is recorded as head and neck disease[2].
- autosomal dominant nonsyndromic deafness 13's instance of is recorded as rare disease[3].
- autosomal dominant nonsyndromic deafness 13's instance of is recorded as class of disease[4].
- autosomal dominant nonsyndromic deafness 13's subclass of is recorded as autosomal dominant nonsyndromic deafness[5].
- autosomal dominant nonsyndromic deafness 13's MeSH descriptor ID is recorded as C566612[6].
- autosomal dominant nonsyndromic deafness 13's OMIM ID is recorded as 601868[7].
- autosomal dominant nonsyndromic deafness 13's Disease Ontology ID is recorded as DOID:0110545[8].
- autosomal dominant nonsyndromic deafness 13's genetic association is recorded as COL11A2[9].
- autosomal dominant nonsyndromic deafness 13's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110545[10].
- autosomal dominant nonsyndromic deafness 13's exact match is recorded as http://identifiers.org/doid/DOID:0110545[11].
- autosomal dominant nonsyndromic deafness 13's UMLS CUI is recorded as C1866095[12].
- autosomal dominant nonsyndromic deafness 13's ICD-10-CM is recorded as H90.3[13].
- autosomal dominant nonsyndromic deafness 13's on focus list of Wikimedia project is recorded as WikiProject Medicine[14].
- autosomal dominant nonsyndromic deafness 13's Mondo ID is recorded as MONDO_0011159[15].
- autosomal dominant nonsyndromic deafness 13's UniProt disease ID is recorded as DI-00843[16].