autosomal dominant nonsyndromic deafness 2B
autosomal dominant nonsyndromic deafness that is characterized postlingual onset in the fourth decade of life with by high frequency progressive hearing loss and has material basis in mutation in the GJB3 gene on chromosome 1p34.3
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autosomal dominant nonsyndromic deafness 2B
Summary
autosomal dominant nonsyndromic deafness 2B is a head and neck disease[1].
Key Facts
- autosomal dominant nonsyndromic deafness 2B's instance of is recorded as head and neck disease[2].
- autosomal dominant nonsyndromic deafness 2B's instance of is recorded as rare disease[3].
- autosomal dominant nonsyndromic deafness 2B's instance of is recorded as class of disease[4].
- autosomal dominant nonsyndromic deafness 2B's subclass of is recorded as autosomal dominant nonsyndromic deafness[5].
- autosomal dominant nonsyndromic deafness 2B's MeSH descriptor ID is recorded as C567214[6].
- autosomal dominant nonsyndromic deafness 2B's OMIM ID is recorded as 612644[7].
- autosomal dominant nonsyndromic deafness 2B's Disease Ontology ID is recorded as DOID:0110559[8].
- autosomal dominant nonsyndromic deafness 2B's genetic association is recorded as GJB3[9].
- autosomal dominant nonsyndromic deafness 2B's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110559[10].
- autosomal dominant nonsyndromic deafness 2B's exact match is recorded as http://identifiers.org/doid/DOID:0110559[11].
- autosomal dominant nonsyndromic deafness 2B's UMLS CUI is recorded as C2675236[12].
- autosomal dominant nonsyndromic deafness 2B's ICD-10-CM is recorded as H90.3[13].
- autosomal dominant nonsyndromic deafness 2B's on focus list of Wikimedia project is recorded as WikiProject Medicine[14].
- autosomal dominant nonsyndromic deafness 2B's Mondo ID is recorded as MONDO_0012976[15].
- autosomal dominant nonsyndromic deafness 2B's UniProt disease ID is recorded as DI-00833[16].