autosomal dominant nonsyndromic deafness 36
autosomal dominant nonsyndromic deafness that is characterized by postlingual onset with flat or gently downsloping audioprofiles and has material basis in mutation in the TMC1 gene on chromosome 9q21
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autosomal dominant nonsyndromic deafness 36
Summary
autosomal dominant nonsyndromic deafness 36 is a head and neck disease[1].
Key Facts
- autosomal dominant nonsyndromic deafness 36's instance of is recorded as head and neck disease[2].
- autosomal dominant nonsyndromic deafness 36's instance of is recorded as rare disease[3].
- autosomal dominant nonsyndromic deafness 36's instance of is recorded as class of disease[4].
- autosomal dominant nonsyndromic deafness 36's subclass of is recorded as autosomal dominant nonsyndromic deafness[5].
- autosomal dominant nonsyndromic deafness 36's MeSH descriptor ID is recorded as C564675[6].
- autosomal dominant nonsyndromic deafness 36's OMIM ID is recorded as 606705[7].
- autosomal dominant nonsyndromic deafness 36's Disease Ontology ID is recorded as DOID:0110563[8].
- autosomal dominant nonsyndromic deafness 36's NCI Thesaurus ID is recorded as C174444[9].
- autosomal dominant nonsyndromic deafness 36's genetic association is recorded as TMC1[10].
- autosomal dominant nonsyndromic deafness 36's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110563[11].
- autosomal dominant nonsyndromic deafness 36's exact match is recorded as http://identifiers.org/doid/DOID:0110563[12].
- autosomal dominant nonsyndromic deafness 36's UMLS CUI is recorded as C1847626[13].
- autosomal dominant nonsyndromic deafness 36's ICD-10-CM is recorded as H90.3[14].
- autosomal dominant nonsyndromic deafness 36's on focus list of Wikimedia project is recorded as WikiProject Medicine[15].
- autosomal dominant nonsyndromic deafness 36's Mondo ID is recorded as MONDO_0011708[16].
- autosomal dominant nonsyndromic deafness 36's UniProt disease ID is recorded as DI-00850[17].