autosomal recessive nonsyndromic deafness 3
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 MYO15A gene on chromosome 17p11
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autosomal recessive nonsyndromic deafness 3
Summary
autosomal recessive nonsyndromic deafness 3 is a head and neck disease[1].
Key Facts
- autosomal recessive nonsyndromic deafness 3's instance of is recorded as head and neck disease[2].
- autosomal recessive nonsyndromic deafness 3's instance of is recorded as rare disease[3].
- autosomal recessive nonsyndromic deafness 3's instance of is recorded as class of disease[4].
- autosomal recessive nonsyndromic deafness 3's subclass of is recorded as autosomal recessive nonsyndromic deafness[5].
- autosomal recessive nonsyndromic deafness 3's MeSH descriptor ID is recorded as C563961[6].
- autosomal recessive nonsyndromic deafness 3's OMIM ID is recorded as 600316[7].
- autosomal recessive nonsyndromic deafness 3's Disease Ontology ID is recorded as DOID:0110488[8].
- autosomal recessive nonsyndromic deafness 3's genetic association is recorded as MYO15A[9].
- autosomal recessive nonsyndromic deafness 3's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110488[10].
- autosomal recessive nonsyndromic deafness 3's exact match is recorded as http://identifiers.org/doid/DOID:0110488[11].
- autosomal recessive nonsyndromic deafness 3's UMLS CUI is recorded as C1838263[12].
- autosomal recessive nonsyndromic deafness 3's ICD-10-CM is recorded as H90.3[13].
- autosomal recessive nonsyndromic deafness 3's on focus list of Wikimedia project is recorded as WikiProject Medicine[14].
- autosomal recessive nonsyndromic deafness 3's Mondo ID is recorded as MONDO_0010860[15].
- autosomal recessive nonsyndromic deafness 3's UniProt disease ID is recorded as DI-00855[16].