autosomal dominant nonsyndromic deafness 17
autosomal dominant nonsyndromic deafness that is characterized by postlingual onset with high frequency progressive hearing loss and has material basis in mutation in the MYH9 gene on chromosome 22q12
Press Enter · cited answer in seconds
0 sources
autosomal dominant nonsyndromic deafness 17
Summary
autosomal dominant nonsyndromic deafness 17 is a head and neck disease[1].
Key Facts
- autosomal dominant nonsyndromic deafness 17's instance of is recorded as head and neck disease[2].
- autosomal dominant nonsyndromic deafness 17's instance of is recorded as rare disease[3].
- autosomal dominant nonsyndromic deafness 17's instance of is recorded as class of disease[4].
- autosomal dominant nonsyndromic deafness 17's subclass of is recorded as autosomal dominant nonsyndromic deafness[5].
- autosomal dominant nonsyndromic deafness 17's OMIM ID is recorded as 603622[6].
- autosomal dominant nonsyndromic deafness 17's Disease Ontology ID is recorded as DOID:0110548[7].
- autosomal dominant nonsyndromic deafness 17's genetic association is recorded as MYH9[8].
- autosomal dominant nonsyndromic deafness 17's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110548[9].
- autosomal dominant nonsyndromic deafness 17's exact match is recorded as http://identifiers.org/doid/DOID:0110548[10].
- autosomal dominant nonsyndromic deafness 17's UMLS CUI is recorded as C1863660[11].
- autosomal dominant nonsyndromic deafness 17's UMLS CUI is recorded as C1863659[12].
- autosomal dominant nonsyndromic deafness 17's ICD-10-CM is recorded as H90.3[13].
- autosomal dominant nonsyndromic deafness 17's on focus list of Wikimedia project is recorded as WikiProject Medicine[14].
- autosomal dominant nonsyndromic deafness 17's Mondo ID is recorded as MONDO_0011350[15].
- autosomal dominant nonsyndromic deafness 17's UniProt disease ID is recorded as DI-00845[16].