autosomal recessive nonsyndromic deafness 9
autosomal recessive nonsyndromic deafness that is characterized by prelingual onset with usually severe to profound, stable hearing loss and has material basis in mutation in the OTOF gene on chromosome 2p23
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autosomal recessive nonsyndromic deafness 9
Summary
autosomal recessive nonsyndromic deafness 9 is a head and neck disease[1].
Key Facts
- autosomal recessive nonsyndromic deafness 9's instance of is recorded as head and neck disease[2].
- autosomal recessive nonsyndromic deafness 9's instance of is recorded as rare disease[3].
- autosomal recessive nonsyndromic deafness 9's instance of is recorded as class of disease[4].
- autosomal recessive nonsyndromic deafness 9's subclass of is recorded as autosomal recessive nonsyndromic deafness[5].
- autosomal recessive nonsyndromic deafness 9's OMIM ID is recorded as 601071[6].
- autosomal recessive nonsyndromic deafness 9's Disease Ontology ID is recorded as DOID:0110535[7].
- autosomal recessive nonsyndromic deafness 9's genetic association is recorded as OTOF[8].
- autosomal recessive nonsyndromic deafness 9's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110535[9].
- autosomal recessive nonsyndromic deafness 9's exact match is recorded as http://identifiers.org/doid/DOID:0110535[10].
- autosomal recessive nonsyndromic deafness 9's UMLS CUI is recorded as C1832828[11].
- autosomal recessive nonsyndromic deafness 9's UMLS CUI is recorded as C1832830[12].
- autosomal recessive nonsyndromic deafness 9's ICD-10-CM is recorded as H90.3[13].
- autosomal recessive nonsyndromic deafness 9's on focus list of Wikimedia project is recorded as WikiProject Medicine[14].
- autosomal recessive nonsyndromic deafness 9's Mondo ID is recorded as MONDO_0010986[15].
- autosomal recessive nonsyndromic deafness 9's UniProt disease ID is recorded as DI-00860[16].