autosomal recessive nonsyndromic deafness 79
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 TPRN gene on chromosome 9q34
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autosomal recessive nonsyndromic deafness 79
Summary
autosomal recessive nonsyndromic deafness 79 is a head and neck disease[1].
Key Facts
- autosomal recessive nonsyndromic deafness 79's instance of is recorded as head and neck disease[2].
- autosomal recessive nonsyndromic deafness 79's instance of is recorded as rare disease[3].
- autosomal recessive nonsyndromic deafness 79's instance of is recorded as class of disease[4].
- autosomal recessive nonsyndromic deafness 79's subclass of is recorded as autosomal recessive nonsyndromic deafness[5].
- autosomal recessive nonsyndromic deafness 79's MeSH descriptor ID is recorded as C567651[6].
- autosomal recessive nonsyndromic deafness 79's OMIM ID is recorded as 613307[7].
- autosomal recessive nonsyndromic deafness 79's Disease Ontology ID is recorded as DOID:0110526[8].
- autosomal recessive nonsyndromic deafness 79's genetic association is recorded as TPRN[9].
- autosomal recessive nonsyndromic deafness 79's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110526[10].
- autosomal recessive nonsyndromic deafness 79's exact match is recorded as http://identifiers.org/doid/DOID:0110526[11].
- autosomal recessive nonsyndromic deafness 79's UMLS CUI is recorded as C2750082[12].
- autosomal recessive nonsyndromic deafness 79's ICD-10-CM is recorded as H90.3[13].
- autosomal recessive nonsyndromic deafness 79's on focus list of Wikimedia project is recorded as WikiProject Medicine[14].
- autosomal recessive nonsyndromic deafness 79's Mondo ID is recorded as MONDO_0013215[15].
- autosomal recessive nonsyndromic deafness 79's UniProt disease ID is recorded as DI-02596[16].