autosomal dominant nonsyndromic deafness 56
autosomal dominant nonsyndromic deafness that has material basis in mutation in the TNC gene on chromosome 9q33
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autosomal dominant nonsyndromic deafness 56
Summary
autosomal dominant nonsyndromic deafness 56 is a head and neck disease[1].
Key Facts
- autosomal dominant nonsyndromic deafness 56's instance of is recorded as head and neck disease[2].
- autosomal dominant nonsyndromic deafness 56's instance of is recorded as rare disease[3].
- autosomal dominant nonsyndromic deafness 56's instance of is recorded as class of disease[4].
- autosomal dominant nonsyndromic deafness 56's subclass of is recorded as autosomal dominant nonsyndromic deafness[5].
- autosomal dominant nonsyndromic deafness 56's OMIM ID is recorded as 615629[6].
- autosomal dominant nonsyndromic deafness 56's Disease Ontology ID is recorded as DOID:0110581[7].
- autosomal dominant nonsyndromic deafness 56's genetic association is recorded as TNC[8].
- autosomal dominant nonsyndromic deafness 56's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110581[9].
- autosomal dominant nonsyndromic deafness 56's exact match is recorded as http://identifiers.org/doid/DOID:0110581[10].
- autosomal dominant nonsyndromic deafness 56's UMLS CUI is recorded as C3810170[11].
- autosomal dominant nonsyndromic deafness 56's ICD-10-CM is recorded as H90.3[12].
- autosomal dominant nonsyndromic deafness 56's on focus list of Wikimedia project is recorded as WikiProject Medicine[13].
- autosomal dominant nonsyndromic deafness 56's Mondo ID is recorded as MONDO_0014283[14].
- autosomal dominant nonsyndromic deafness 56's UniProt disease ID is recorded as DI-04030[15].