autosomal dominant nonsyndromic deafness 23
autosomal dominant nonsyndromic deafness that is characterized by prelingual onset with high frequency progressive hearing loss and has material basis in mutation in the SIX1 gene on chromosome 14q23
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autosomal dominant nonsyndromic deafness 23
Summary
autosomal dominant nonsyndromic deafness 23 is a head and neck disease[1].
Key Facts
- autosomal dominant nonsyndromic deafness 23's instance of is recorded as head and neck disease[2].
- autosomal dominant nonsyndromic deafness 23's instance of is recorded as rare disease[3].
- autosomal dominant nonsyndromic deafness 23's instance of is recorded as class of disease[4].
- autosomal dominant nonsyndromic deafness 23's subclass of is recorded as autosomal dominant nonsyndromic deafness[5].
- autosomal dominant nonsyndromic deafness 23's MeSH descriptor ID is recorded as C565357[6].
- autosomal dominant nonsyndromic deafness 23's OMIM ID is recorded as 605192[7].
- autosomal dominant nonsyndromic deafness 23's Disease Ontology ID is recorded as DOID:0110553[8].
- autosomal dominant nonsyndromic deafness 23's genetic association is recorded as SIX1[9].
- autosomal dominant nonsyndromic deafness 23's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110553[10].
- autosomal dominant nonsyndromic deafness 23's exact match is recorded as http://identifiers.org/doid/DOID:0110553[11].
- autosomal dominant nonsyndromic deafness 23's UMLS CUI is recorded as C1854594[12].
- autosomal dominant nonsyndromic deafness 23's ICD-10-CM is recorded as H90.3[13].
- autosomal dominant nonsyndromic deafness 23's on focus list of Wikimedia project is recorded as WikiProject Medicine[14].
- autosomal dominant nonsyndromic deafness 23's Mondo ID is recorded as MONDO_0011519[15].
- autosomal dominant nonsyndromic deafness 23's UniProt disease ID is recorded as DI-01205[16].