autosomal recessive nonsyndromic deafness 37
autosomal recessive nonsyndromic deafness that is characterized by prelingual onset and has material basis in mutation in the MYO6 gene on chromosome 6q14
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autosomal recessive nonsyndromic deafness 37
Summary
autosomal recessive nonsyndromic deafness 37 is a head and neck disease[1].
Key Facts
- autosomal recessive nonsyndromic deafness 37's instance of is recorded as head and neck disease[2].
- autosomal recessive nonsyndromic deafness 37's instance of is recorded as rare disease[3].
- autosomal recessive nonsyndromic deafness 37's instance of is recorded as class of disease[4].
- autosomal recessive nonsyndromic deafness 37's subclass of is recorded as autosomal recessive nonsyndromic deafness[5].
- autosomal recessive nonsyndromic deafness 37's MeSH descriptor ID is recorded as C564331[6].
- autosomal recessive nonsyndromic deafness 37's OMIM ID is recorded as 607821[7].
- autosomal recessive nonsyndromic deafness 37's Disease Ontology ID is recorded as DOID:0110495[8].
- autosomal recessive nonsyndromic deafness 37's genetic association is recorded as MYO6[9].
- autosomal recessive nonsyndromic deafness 37's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110495[10].
- autosomal recessive nonsyndromic deafness 37's exact match is recorded as http://identifiers.org/doid/DOID:0110495[11].
- autosomal recessive nonsyndromic deafness 37's UMLS CUI is recorded as C1843028[12].
- autosomal recessive nonsyndromic deafness 37's ICD-10-CM is recorded as H90.3[13].
- autosomal recessive nonsyndromic deafness 37's on focus list of Wikimedia project is recorded as WikiProject Medicine[14].
- autosomal recessive nonsyndromic deafness 37's Mondo ID is recorded as MONDO_0011912[15].
- autosomal recessive nonsyndromic deafness 37's UniProt disease ID is recorded as DI-00874[16].