autosomal recessive nonsyndromic deafness 7
autosomal recessive nonsyndromic deafness that is characterized by prelingual onset with severe to profound, stable hearing loss and has material basis in mutation in the TMC1 gene on chromosome 9q21
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autosomal recessive nonsyndromic deafness 7
Summary
autosomal recessive nonsyndromic deafness 7 is a head and neck disease[1].
Key Facts
- autosomal recessive nonsyndromic deafness 7's instance of is recorded as head and neck disease[2].
- autosomal recessive nonsyndromic deafness 7's instance of is recorded as rare disease[3].
- autosomal recessive nonsyndromic deafness 7's instance of is recorded as class of disease[4].
- autosomal recessive nonsyndromic deafness 7's subclass of is recorded as autosomal recessive nonsyndromic deafness[5].
- autosomal recessive nonsyndromic deafness 7's MeSH descriptor ID is recorded as C563417[6].
- autosomal recessive nonsyndromic deafness 7's OMIM ID is recorded as 600974[7].
- autosomal recessive nonsyndromic deafness 7's Disease Ontology ID is recorded as DOID:0110520[8].
- autosomal recessive nonsyndromic deafness 7's genetic association is recorded as TMC1[9].
- autosomal recessive nonsyndromic deafness 7's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110520[10].
- autosomal recessive nonsyndromic deafness 7's exact match is recorded as http://identifiers.org/doid/DOID:0110520[11].
- autosomal recessive nonsyndromic deafness 7's UMLS CUI is recorded as C1832978[12].
- autosomal recessive nonsyndromic deafness 7's ICD-10-CM is recorded as H90.3[13].
- autosomal recessive nonsyndromic deafness 7's on focus list of Wikimedia project is recorded as WikiProject Medicine[14].
- autosomal recessive nonsyndromic deafness 7's Mondo ID is recorded as MONDO_0010967[15].
- autosomal recessive nonsyndromic deafness 7's UniProt disease ID is recorded as DI-00858[16].