autosomal recessive nonsyndromic deafness 97
autosomal recessive nonsyndromic deafness that has material basis in mutation in the MET gene on chromosome 7q31
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autosomal recessive nonsyndromic deafness 97
Summary
autosomal recessive nonsyndromic deafness 97 is a head and neck disease[1].
Key Facts
- autosomal recessive nonsyndromic deafness 97's instance of is recorded as head and neck disease[2].
- autosomal recessive nonsyndromic deafness 97's instance of is recorded as rare disease[3].
- autosomal recessive nonsyndromic deafness 97's instance of is recorded as class of disease[4].
- autosomal recessive nonsyndromic deafness 97's subclass of is recorded as autosomal recessive nonsyndromic deafness[5].
- autosomal recessive nonsyndromic deafness 97's OMIM ID is recorded as 616705[6].
- autosomal recessive nonsyndromic deafness 97's Disease Ontology ID is recorded as DOID:0110539[7].
- autosomal recessive nonsyndromic deafness 97's genetic association is recorded as MET[8].
- autosomal recessive nonsyndromic deafness 97's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110539[9].
- autosomal recessive nonsyndromic deafness 97's exact match is recorded as http://identifiers.org/doid/DOID:0110539[10].
- autosomal recessive nonsyndromic deafness 97's UMLS CUI is recorded as C4084709[11].
- autosomal recessive nonsyndromic deafness 97's ICD-10-CM is recorded as H90.3[12].
- autosomal recessive nonsyndromic deafness 97's on focus list of Wikimedia project is recorded as WikiProject Medicine[13].
- autosomal recessive nonsyndromic deafness 97's Mondo ID is recorded as MONDO_0014739[14].
- autosomal recessive nonsyndromic deafness 97's UniProt disease ID is recorded as DI-04599[15].