autosomal dominant nonsyndromic deafness 3B
autosomal dominant nonsyndromic deafness that has material basis in mutation in the GJB6 gene on chromosome 13q12
Press Enter · cited answer in seconds
0 sources
autosomal dominant nonsyndromic deafness 3B
Summary
autosomal dominant nonsyndromic deafness 3B is a head and neck disease[1].
Key Facts
- autosomal dominant nonsyndromic deafness 3B's instance of is recorded as head and neck disease[2].
- autosomal dominant nonsyndromic deafness 3B's instance of is recorded as rare disease[3].
- autosomal dominant nonsyndromic deafness 3B's instance of is recorded as class of disease[4].
- autosomal dominant nonsyndromic deafness 3B's subclass of is recorded as autosomal dominant nonsyndromic deafness[5].
- autosomal dominant nonsyndromic deafness 3B's MeSH descriptor ID is recorded as C567215[6].
- autosomal dominant nonsyndromic deafness 3B's OMIM ID is recorded as 612643[7].
- autosomal dominant nonsyndromic deafness 3B's Disease Ontology ID is recorded as DOID:0110565[8].
- autosomal dominant nonsyndromic deafness 3B's genetic association is recorded as GJB6[9].
- autosomal dominant nonsyndromic deafness 3B's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110565[10].
- autosomal dominant nonsyndromic deafness 3B's exact match is recorded as http://identifiers.org/doid/DOID:0110565[11].
- autosomal dominant nonsyndromic deafness 3B's UMLS CUI is recorded as C2675237[12].
- autosomal dominant nonsyndromic deafness 3B's ICD-10-CM is recorded as H90.3[13].
- autosomal dominant nonsyndromic deafness 3B's on focus list of Wikimedia project is recorded as WikiProject Medicine[14].
- autosomal dominant nonsyndromic deafness 3B's Mondo ID is recorded as MONDO_0012975[15].
- autosomal dominant nonsyndromic deafness 3B's UniProt disease ID is recorded as DI-00835[16].