autosomal dominant nonsyndromic deafness 12
autosomal dominant nonsyndromic deafness that is characterized by prelingual onset and mid-frequency hearing loss and has material basis in mutation in the TECTA gene on chromosome 11q23
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autosomal dominant nonsyndromic deafness 12
Summary
autosomal dominant nonsyndromic deafness 12 is a head and neck disease[1].
Key Facts
- autosomal dominant nonsyndromic deafness 12's instance of is recorded as head and neck disease[2].
- autosomal dominant nonsyndromic deafness 12's instance of is recorded as rare disease[3].
- autosomal dominant nonsyndromic deafness 12's instance of is recorded as class of disease[4].
- autosomal dominant nonsyndromic deafness 12's subclass of is recorded as autosomal dominant nonsyndromic deafness[5].
- autosomal dominant nonsyndromic deafness 12's MeSH descriptor ID is recorded as C563295[6].
- autosomal dominant nonsyndromic deafness 12's OMIM ID is recorded as 601543[7].
- autosomal dominant nonsyndromic deafness 12's Disease Ontology ID is recorded as DOID:0110544[8].
- autosomal dominant nonsyndromic deafness 12's genetic association is recorded as TECTA[9].
- autosomal dominant nonsyndromic deafness 12's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110544[10].
- autosomal dominant nonsyndromic deafness 12's exact match is recorded as http://identifiers.org/doid/DOID:0110544[11].
- autosomal dominant nonsyndromic deafness 12's UMLS CUI is recorded as C1832187[12].
- autosomal dominant nonsyndromic deafness 12's ICD-10-CM is recorded as H90.3[13].
- autosomal dominant nonsyndromic deafness 12's on focus list of Wikimedia project is recorded as WikiProject Medicine[14].
- autosomal dominant nonsyndromic deafness 12's Mondo ID is recorded as MONDO_0011102[15].
- autosomal dominant nonsyndromic deafness 12's UniProt disease ID is recorded as DI-00842[16].