autosomal recessive nonsyndromic deafness 48
autosomal recessive nonsyndromic deafness that has material basis in mutation in the CIB2 gene on chromosome 15q25
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autosomal recessive nonsyndromic deafness 48
Summary
autosomal recessive nonsyndromic deafness 48 is a head and neck disease[1].
Key Facts
- autosomal recessive nonsyndromic deafness 48's instance of is recorded as head and neck disease[2].
- autosomal recessive nonsyndromic deafness 48's instance of is recorded as rare disease[3].
- autosomal recessive nonsyndromic deafness 48's instance of is recorded as class of disease[4].
- autosomal recessive nonsyndromic deafness 48's subclass of is recorded as autosomal recessive nonsyndromic deafness[5].
- autosomal recessive nonsyndromic deafness 48's MeSH descriptor ID is recorded as C563720[6].
- autosomal recessive nonsyndromic deafness 48's OMIM ID is recorded as 609439[7].
- autosomal recessive nonsyndromic deafness 48's Disease Ontology ID is recorded as DOID:0110505[8].
- autosomal recessive nonsyndromic deafness 48's genetic association is recorded as CIB2[9].
- autosomal recessive nonsyndromic deafness 48's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110505[10].
- autosomal recessive nonsyndromic deafness 48's exact match is recorded as http://identifiers.org/doid/DOID:0110505[11].
- autosomal recessive nonsyndromic deafness 48's UMLS CUI is recorded as C1836199[12].
- autosomal recessive nonsyndromic deafness 48's ICD-10-CM is recorded as H90.3[13].
- autosomal recessive nonsyndromic deafness 48's on focus list of Wikimedia project is recorded as WikiProject Medicine[14].
- autosomal recessive nonsyndromic deafness 48's Mondo ID is recorded as MONDO_0012273[15].
- autosomal recessive nonsyndromic deafness 48's UniProt disease ID is recorded as DI-03551[16].