autosomal dominant nonsyndromic deafness 25
autosomal dominant nonsyndromic deafness that is characterized by postlingual onset in the second-sixth decade of life with high frequency progressive hearing loss and has material basis in mutation in the SLC17A8 gene on chromosome 12q23
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Summary
autosomal dominant nonsyndromic deafness 25 is a rare disease[1].
Key Facts
- autosomal dominant nonsyndromic deafness 25's instance of is recorded as rare disease[2].
- autosomal dominant nonsyndromic deafness 25's instance of is recorded as class of disease[3].
- autosomal dominant nonsyndromic deafness 25's subclass of is recorded as autosomal dominant nonsyndromic deafness[4].
- autosomal dominant nonsyndromic deafness 25's MeSH descriptor ID is recorded as C565319[5].
- autosomal dominant nonsyndromic deafness 25's OMIM ID is recorded as 605583[6].
- autosomal dominant nonsyndromic deafness 25's Disease Ontology ID is recorded as DOID:0110555[7].
- autosomal dominant nonsyndromic deafness 25's genetic association is recorded as SLC17A8[8].
- autosomal dominant nonsyndromic deafness 25's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110555[9].
- autosomal dominant nonsyndromic deafness 25's exact match is recorded as http://identifiers.org/doid/DOID:0110555[10].
- autosomal dominant nonsyndromic deafness 25's UMLS CUI is recorded as C1854158[11].
- autosomal dominant nonsyndromic deafness 25's ICD-10-CM is recorded as H90.3[12].
- autosomal dominant nonsyndromic deafness 25's on focus list of Wikimedia project is recorded as WikiProject Medicine[13].
- autosomal dominant nonsyndromic deafness 25's Mondo ID is recorded as MONDO_0011568[14].
- autosomal dominant nonsyndromic deafness 25's UniProt disease ID is recorded as DI-00848[15].