autosomal recessive nonsyndromic deafness 15
autosomal recessive nonsyndromic deafness that has material basis in mutation in the GIPC3 gene on chromosome 19p13
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autosomal recessive nonsyndromic deafness 15
Summary
autosomal recessive nonsyndromic deafness 15 is a head and neck disease[1].
Key Facts
- autosomal recessive nonsyndromic deafness 15's instance of is recorded as head and neck disease[2].
- autosomal recessive nonsyndromic deafness 15's instance of is recorded as rare disease[3].
- autosomal recessive nonsyndromic deafness 15's instance of is recorded as class of disease[4].
- autosomal recessive nonsyndromic deafness 15's subclass of is recorded as autosomal recessive nonsyndromic deafness[5].
- autosomal recessive nonsyndromic deafness 15's MeSH descriptor ID is recorded as C566611[6].
- autosomal recessive nonsyndromic deafness 15's OMIM ID is recorded as 601869[7].
- autosomal recessive nonsyndromic deafness 15's Disease Ontology ID is recorded as DOID:0110470[8].
- autosomal recessive nonsyndromic deafness 15's genetic association is recorded as GIPC3[9].
- autosomal recessive nonsyndromic deafness 15's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110470[10].
- autosomal recessive nonsyndromic deafness 15's exact match is recorded as http://identifiers.org/doid/DOID:0110470[11].
- autosomal recessive nonsyndromic deafness 15's UMLS CUI is recorded as C1866094[12].
- autosomal recessive nonsyndromic deafness 15's ICD-10-CM is recorded as H90.3[13].
- autosomal recessive nonsyndromic deafness 15's on focus list of Wikimedia project is recorded as WikiProject Medicine[14].
- autosomal recessive nonsyndromic deafness 15's Mondo ID is recorded as MONDO_0011160[15].
- autosomal recessive nonsyndromic deafness 15's UniProt disease ID is recorded as DI-03190[16].