autosomal dominant nonsyndromic deafness 6
autosomal dominant nonsyndromic deafness that is characterized by prelingual onset and low frequency progressive hearing loss and has material basis in mutation in the WFS1 gene on chromosome 4p16
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autosomal dominant nonsyndromic deafness 6
Summary
autosomal dominant nonsyndromic deafness 6 is a rare disease[1].
Key Facts
- autosomal dominant nonsyndromic deafness 6's instance of is recorded as rare disease[2].
- autosomal dominant nonsyndromic deafness 6's instance of is recorded as class of disease[3].
- autosomal dominant nonsyndromic deafness 6's subclass of is recorded as autosomal dominant nonsyndromic deafness[4].
- autosomal dominant nonsyndromic deafness 6's MeSH descriptor ID is recorded as C563421[5].
- autosomal dominant nonsyndromic deafness 6's OMIM ID is recorded as 600965[6].
- autosomal dominant nonsyndromic deafness 6's Disease Ontology ID is recorded as DOID:0110584[7].
- autosomal dominant nonsyndromic deafness 6's genetic association is recorded as WFS1[8].
- autosomal dominant nonsyndromic deafness 6's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110584[9].
- autosomal dominant nonsyndromic deafness 6's exact match is recorded as http://identifiers.org/doid/DOID:0110584[10].
- autosomal dominant nonsyndromic deafness 6's UMLS CUI is recorded as C1833021[11].
- autosomal dominant nonsyndromic deafness 6's ICD-10-CM is recorded as H90.3[12].
- autosomal dominant nonsyndromic deafness 6's on focus list of Wikimedia project is recorded as WikiProject Medicine[13].
- autosomal dominant nonsyndromic deafness 6's Mondo ID is recorded as MONDO_0010963[14].
- autosomal dominant nonsyndromic deafness 6's UniProt disease ID is recorded as DI-00838[15].