autosomal recessive nonsyndromic deafness 76
autosomal recessive nonsyndromic deafness that is characterized by prelingual onset with high frequency, progressive hearing loss and has material basis in mutation in the SYNE4 gene on chromosome 19q13
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Summary
autosomal recessive nonsyndromic deafness 76 is a rare disease[1].
Key Facts
- autosomal recessive nonsyndromic deafness 76's instance of is recorded as rare disease[2].
- autosomal recessive nonsyndromic deafness 76's instance of is recorded as class of disease[3].
- autosomal recessive nonsyndromic deafness 76's subclass of is recorded as autosomal recessive nonsyndromic deafness[4].
- autosomal recessive nonsyndromic deafness 76's OMIM ID is recorded as 615540[5].
- autosomal recessive nonsyndromic deafness 76's Disease Ontology ID is recorded as DOID:0110524[6].
- autosomal recessive nonsyndromic deafness 76's genetic association is recorded as SYNE4[7].
- autosomal recessive nonsyndromic deafness 76's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110524[8].
- autosomal recessive nonsyndromic deafness 76's exact match is recorded as http://identifiers.org/doid/DOID:0110524[9].
- autosomal recessive nonsyndromic deafness 76's UMLS CUI is recorded as C3147083[10].
- autosomal recessive nonsyndromic deafness 76's ICD-10-CM is recorded as H90.3[11].
- autosomal recessive nonsyndromic deafness 76's on focus list of Wikimedia project is recorded as WikiProject Medicine[12].
- autosomal recessive nonsyndromic deafness 76's Mondo ID is recorded as MONDO_0014237[13].
- autosomal recessive nonsyndromic deafness 76's UniProt disease ID is recorded as DI-03957[14].