autosomal recessive nonsyndromic deafness 31
autosomal recessive nonsyndromic deafness that is characterized by prelingual onset and has material basis in mutation in the WHRN gene on chromosome 9q32
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autosomal recessive nonsyndromic deafness 31
Summary
autosomal recessive nonsyndromic deafness 31 is a head and neck disease[1].
Key Facts
- autosomal recessive nonsyndromic deafness 31's instance of is recorded as head and neck disease[2].
- autosomal recessive nonsyndromic deafness 31's instance of is recorded as rare disease[3].
- autosomal recessive nonsyndromic deafness 31's instance of is recorded as class of disease[4].
- autosomal recessive nonsyndromic deafness 31's subclass of is recorded as autosomal recessive nonsyndromic deafness[5].
- autosomal recessive nonsyndromic deafness 31's MeSH descriptor ID is recorded as C564629[6].
- autosomal recessive nonsyndromic deafness 31's OMIM ID is recorded as 607084[7].
- autosomal recessive nonsyndromic deafness 31's Disease Ontology ID is recorded as DOID:0110490[8].
- autosomal recessive nonsyndromic deafness 31's genetic association is recorded as WHRN[9].
- autosomal recessive nonsyndromic deafness 31's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110490[10].
- autosomal recessive nonsyndromic deafness 31's exact match is recorded as http://identifiers.org/doid/DOID:0110490[11].
- autosomal recessive nonsyndromic deafness 31's UMLS CUI is recorded as C1846839[12].
- autosomal recessive nonsyndromic deafness 31's ICD-10-CM is recorded as H90.3[13].
- autosomal recessive nonsyndromic deafness 31's on focus list of Wikimedia project is recorded as WikiProject Medicine[14].
- autosomal recessive nonsyndromic deafness 31's Mondo ID is recorded as MONDO_0011767[15].
- autosomal recessive nonsyndromic deafness 31's UniProt disease ID is recorded as DI-00871[16].