autosomal dominant nonsyndromic deafness 44
autosomal dominant nonsyndromic deafness that is characterized postlingual onset with low to mild frequency progressive hearing loss and has material basis in mutation in the CCDC50 gene on chromosome 3q28
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Summary
autosomal dominant nonsyndromic deafness 44 is a rare disease[1].
Key Facts
- autosomal dominant nonsyndromic deafness 44's instance of is recorded as rare disease[2].
- autosomal dominant nonsyndromic deafness 44's instance of is recorded as class of disease[3].
- autosomal dominant nonsyndromic deafness 44's subclass of is recorded as autosomal dominant nonsyndromic deafness[4].
- autosomal dominant nonsyndromic deafness 44's MeSH descriptor ID is recorded as C564399[5].
- autosomal dominant nonsyndromic deafness 44's OMIM ID is recorded as 607453[6].
- autosomal dominant nonsyndromic deafness 44's Disease Ontology ID is recorded as DOID:0110569[7].
- autosomal dominant nonsyndromic deafness 44's genetic association is recorded as CCDC50[8].
- autosomal dominant nonsyndromic deafness 44's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110569[9].
- autosomal dominant nonsyndromic deafness 44's exact match is recorded as http://identifiers.org/doid/DOID:0110569[10].
- autosomal dominant nonsyndromic deafness 44's UMLS CUI is recorded as C1843895[11].
- autosomal dominant nonsyndromic deafness 44's ICD-10-CM is recorded as H90.3[12].
- autosomal dominant nonsyndromic deafness 44's on focus list of Wikimedia project is recorded as WikiProject Medicine[13].
- autosomal dominant nonsyndromic deafness 44's Mondo ID is recorded as MONDO_0011832[14].
- autosomal dominant nonsyndromic deafness 44's UniProt disease ID is recorded as DI-01220[15].