autosomal recessive nonsyndromic deafness 22
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 OTOA gene on chromosome 16p12
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autosomal recessive nonsyndromic deafness 22
Summary
autosomal recessive nonsyndromic deafness 22 is a head and neck disease[1].
Key Facts
- autosomal recessive nonsyndromic deafness 22's instance of is recorded as head and neck disease[2].
- autosomal recessive nonsyndromic deafness 22's instance of is recorded as rare disease[3].
- autosomal recessive nonsyndromic deafness 22's instance of is recorded as class of disease[4].
- autosomal recessive nonsyndromic deafness 22's subclass of is recorded as autosomal recessive nonsyndromic deafness[5].
- autosomal recessive nonsyndromic deafness 22's MeSH descriptor ID is recorded as C564633[6].
- autosomal recessive nonsyndromic deafness 22's OMIM ID is recorded as 607039[7].
- autosomal recessive nonsyndromic deafness 22's Disease Ontology ID is recorded as DOID:0110480[8].
- autosomal recessive nonsyndromic deafness 22's genetic association is recorded as OTOA[9].
- autosomal recessive nonsyndromic deafness 22's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110480[10].
- autosomal recessive nonsyndromic deafness 22's exact match is recorded as http://identifiers.org/doid/DOID:0110480[11].
- autosomal recessive nonsyndromic deafness 22's UMLS CUI is recorded as C1846896[12].
- autosomal recessive nonsyndromic deafness 22's ICD-10-CM is recorded as H90.3[13].
- autosomal recessive nonsyndromic deafness 22's on focus list of Wikimedia project is recorded as WikiProject Medicine[14].
- autosomal recessive nonsyndromic deafness 22's Mondo ID is recorded as MONDO_0011762[15].
- autosomal recessive nonsyndromic deafness 22's UniProt disease ID is recorded as DI-00866[16].