autosomal recessive nonsyndromic deafness 59
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 DFNB59 gene on chromosome 2q31
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autosomal recessive nonsyndromic deafness 59
Summary
autosomal recessive nonsyndromic deafness 59 is a head and neck disease[1].
Key Facts
- autosomal recessive nonsyndromic deafness 59's instance of is recorded as head and neck disease[2].
- autosomal recessive nonsyndromic deafness 59's instance of is recorded as rare disease[3].
- autosomal recessive nonsyndromic deafness 59's instance of is recorded as class of disease[4].
- autosomal recessive nonsyndromic deafness 59's subclass of is recorded as autosomal recessive nonsyndromic deafness[5].
- autosomal recessive nonsyndromic deafness 59's MeSH descriptor ID is recorded as C565698[6].
- autosomal recessive nonsyndromic deafness 59's OMIM ID is recorded as 610220[7].
- autosomal recessive nonsyndromic deafness 59's Disease Ontology ID is recorded as DOID:0110511[8].
- autosomal recessive nonsyndromic deafness 59's genetic association is recorded as PJVK[9].
- autosomal recessive nonsyndromic deafness 59's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110511[10].
- autosomal recessive nonsyndromic deafness 59's exact match is recorded as http://identifiers.org/doid/DOID:0110511[11].
- autosomal recessive nonsyndromic deafness 59's UMLS CUI is recorded as C1857744[12].
- autosomal recessive nonsyndromic deafness 59's ICD-10-CM is recorded as H90.3[13].
- autosomal recessive nonsyndromic deafness 59's on focus list of Wikimedia project is recorded as WikiProject Medicine[14].
- autosomal recessive nonsyndromic deafness 59's Mondo ID is recorded as MONDO_0012445[15].
- autosomal recessive nonsyndromic deafness 59's UniProt disease ID is recorded as DI-00877[16].