autosomal dominant nonsyndromic deafness 28
autosomal dominant nonsyndromic deafness that is characterized by postlingual onset with flat or gently downsloping audioprofiles and has material basis in mutation in the GRHL2 gene on chromosome 8q22
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autosomal dominant nonsyndromic deafness 28
Summary
autosomal dominant nonsyndromic deafness 28 is a rare disease[1].
Key Facts
- autosomal dominant nonsyndromic deafness 28's instance of is recorded as rare disease[2].
- autosomal dominant nonsyndromic deafness 28's instance of is recorded as class of disease[3].
- autosomal dominant nonsyndromic deafness 28's subclass of is recorded as autosomal dominant nonsyndromic deafness[4].
- autosomal dominant nonsyndromic deafness 28's MeSH descriptor ID is recorded as C563890[5].
- autosomal dominant nonsyndromic deafness 28's OMIM ID is recorded as 608641[6].
- autosomal dominant nonsyndromic deafness 28's Disease Ontology ID is recorded as DOID:0110557[7].
- autosomal dominant nonsyndromic deafness 28's genetic association is recorded as GRHL2[8].
- autosomal dominant nonsyndromic deafness 28's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110557[9].
- autosomal dominant nonsyndromic deafness 28's exact match is recorded as http://identifiers.org/doid/DOID:0110557[10].
- autosomal dominant nonsyndromic deafness 28's UMLS CUI is recorded as C1837640[11].
- autosomal dominant nonsyndromic deafness 28's ICD-10-CM is recorded as H90.3[12].
- autosomal dominant nonsyndromic deafness 28's on focus list of Wikimedia project is recorded as WikiProject Medicine[13].
- autosomal dominant nonsyndromic deafness 28's Mondo ID is recorded as MONDO_0012083[14].
- autosomal dominant nonsyndromic deafness 28's UniProt disease ID is recorded as DI-00849[15].