autosomal dominant nonsyndromic deafness 20
autosomal dominant nonsyndromic deafness that is characterized by postlingual onset with high frequency progressive hearing loss and has material basis in mutation in the ACTG1 gene on chromosome 17q25
Press Enter · cited answer in seconds
0 sources
autosomal dominant nonsyndromic deafness 20
Summary
autosomal dominant nonsyndromic deafness 20 is a rare disease[1].
Key Facts
- autosomal dominant nonsyndromic deafness 20's instance of is recorded as rare disease[2].
- autosomal dominant nonsyndromic deafness 20's instance of is recorded as class of disease[3].
- autosomal dominant nonsyndromic deafness 20's subclass of is recorded as autosomal dominant nonsyndromic deafness[4].
- autosomal dominant nonsyndromic deafness 20's MeSH descriptor ID is recorded as C565754[5].
- autosomal dominant nonsyndromic deafness 20's OMIM ID is recorded as 604717[6].
- autosomal dominant nonsyndromic deafness 20's Disease Ontology ID is recorded as DOID:0110550[7].
- autosomal dominant nonsyndromic deafness 20's genetic association is recorded as ACTG1[8].
- autosomal dominant nonsyndromic deafness 20's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110550[9].
- autosomal dominant nonsyndromic deafness 20's exact match is recorded as http://identifiers.org/doid/DOID:0110550[10].
- autosomal dominant nonsyndromic deafness 20's UMLS CUI is recorded as C1858172[11].
- autosomal dominant nonsyndromic deafness 20's ICD-10-CM is recorded as H90.3[12].
- autosomal dominant nonsyndromic deafness 20's on focus list of Wikimedia project is recorded as WikiProject Medicine[13].
- autosomal dominant nonsyndromic deafness 20's Mondo ID is recorded as MONDO_0011480[14].
- autosomal dominant nonsyndromic deafness 20's UniProt disease ID is recorded as DI-00846[15].