autosomal recessive nonsyndromic deafness 77
autosomal recessive nonsyndromic deafness that is characterized by postlingual onset with moderate to profound, progressive hearing loss and has material basis in mutation in the LOXHD1 gene on chromosome 18q21
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autosomal recessive nonsyndromic deafness 77
Summary
autosomal recessive nonsyndromic deafness 77 is a head and neck disease[1].
Key Facts
- autosomal recessive nonsyndromic deafness 77's instance of is recorded as head and neck disease[2].
- autosomal recessive nonsyndromic deafness 77's instance of is recorded as rare disease[3].
- autosomal recessive nonsyndromic deafness 77's instance of is recorded as class of disease[4].
- autosomal recessive nonsyndromic deafness 77's subclass of is recorded as autosomal recessive nonsyndromic deafness[5].
- autosomal recessive nonsyndromic deafness 77's MeSH descriptor ID is recorded as C567543[6].
- autosomal recessive nonsyndromic deafness 77's OMIM ID is recorded as 613079[7].
- autosomal recessive nonsyndromic deafness 77's Disease Ontology ID is recorded as DOID:0110525[8].
- autosomal recessive nonsyndromic deafness 77's genetic association is recorded as LOXHD1[9].
- autosomal recessive nonsyndromic deafness 77's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110525[10].
- autosomal recessive nonsyndromic deafness 77's exact match is recorded as http://identifiers.org/doid/DOID:0110525[11].
- autosomal recessive nonsyndromic deafness 77's UMLS CUI is recorded as C2746083[12].
- autosomal recessive nonsyndromic deafness 77's ICD-10-CM is recorded as H90.3[13].
- autosomal recessive nonsyndromic deafness 77's on focus list of Wikimedia project is recorded as WikiProject Medicine[14].
- autosomal recessive nonsyndromic deafness 77's Mondo ID is recorded as MONDO_0013119[15].
- autosomal recessive nonsyndromic deafness 77's UniProt disease ID is recorded as DI-02528[16].