autosomal recessive nonsyndromic deafness 86
autosomal recessive nonsyndromic deafness that has material basis in mutation in the TBC1D24 gene on chromosome 16p13
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Summary
autosomal recessive nonsyndromic deafness 86 is a rare disease[1].
Key Facts
- autosomal recessive nonsyndromic deafness 86's instance of is recorded as rare disease[2].
- autosomal recessive nonsyndromic deafness 86's instance of is recorded as class of disease[3].
- autosomal recessive nonsyndromic deafness 86's subclass of is recorded as autosomal recessive nonsyndromic deafness[4].
- autosomal recessive nonsyndromic deafness 86's OMIM ID is recorded as 614617[5].
- autosomal recessive nonsyndromic deafness 86's Disease Ontology ID is recorded as DOID:0110532[6].
- autosomal recessive nonsyndromic deafness 86's genetic association is recorded as TBC1D24[7].
- autosomal recessive nonsyndromic deafness 86's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110532[8].
- autosomal recessive nonsyndromic deafness 86's exact match is recorded as http://identifiers.org/doid/DOID:0110532[9].
- autosomal recessive nonsyndromic deafness 86's UMLS CUI is recorded as C2829265[10].
- autosomal recessive nonsyndromic deafness 86's ICD-10-CM is recorded as H90.3[11].
- autosomal recessive nonsyndromic deafness 86's on focus list of Wikimedia project is recorded as WikiProject Medicine[12].
- autosomal recessive nonsyndromic deafness 86's Mondo ID is recorded as MONDO_0013826[13].
- autosomal recessive nonsyndromic deafness 86's UniProt disease ID is recorded as DI-04026[14].