autosomal recessive nonsyndromic deafness 66
autosomal recessive nonsyndromic deafness that has material basis in mutation in the DCDC2 gene on chromosome 6p22
Press Enter · cited answer in seconds
0 sources
autosomal recessive nonsyndromic deafness 66
Summary
autosomal recessive nonsyndromic deafness 66 is a head and neck disease[1].
Key Facts
- autosomal recessive nonsyndromic deafness 66's instance of is recorded as head and neck disease[2].
- autosomal recessive nonsyndromic deafness 66's instance of is recorded as rare disease[3].
- autosomal recessive nonsyndromic deafness 66's instance of is recorded as class of disease[4].
- autosomal recessive nonsyndromic deafness 66's subclass of is recorded as autosomal recessive nonsyndromic deafness[5].
- autosomal recessive nonsyndromic deafness 66's MeSH descriptor ID is recorded as C565701[6].
- autosomal recessive nonsyndromic deafness 66's OMIM ID is recorded as 610212[7].
- autosomal recessive nonsyndromic deafness 66's Disease Ontology ID is recorded as DOID:0110517[8].
- autosomal recessive nonsyndromic deafness 66's genetic association is recorded as DCDC2[9].
- autosomal recessive nonsyndromic deafness 66's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110517[10].
- autosomal recessive nonsyndromic deafness 66's exact match is recorded as http://identifiers.org/doid/DOID:0110517[11].
- autosomal recessive nonsyndromic deafness 66's UMLS CUI is recorded as C1857750[12].
- autosomal recessive nonsyndromic deafness 66's ICD-10-CM is recorded as H90.3[13].
- autosomal recessive nonsyndromic deafness 66's on focus list of Wikimedia project is recorded as WikiProject Medicine[14].
- autosomal recessive nonsyndromic deafness 66's Mondo ID is recorded as MONDO_0012442[15].
- autosomal recessive nonsyndromic deafness 66's UniProt disease ID is recorded as DI-04549[16].