autosomal recessive nonsyndromic deafness 67
autosomal recessive nonsyndromic deafness that is characterized by prelingual onset with severe to profound, stable hearing loss and has material basis in mutation in the LHFPL5 gene on chromosome 6p21
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autosomal recessive nonsyndromic deafness 67
Summary
autosomal recessive nonsyndromic deafness 67 is a head and neck disease[1].
Key Facts
- autosomal recessive nonsyndromic deafness 67's instance of is recorded as head and neck disease[2].
- autosomal recessive nonsyndromic deafness 67's instance of is recorded as rare disease[3].
- autosomal recessive nonsyndromic deafness 67's instance of is recorded as class of disease[4].
- autosomal recessive nonsyndromic deafness 67's subclass of is recorded as autosomal recessive nonsyndromic deafness[5].
- autosomal recessive nonsyndromic deafness 67's MeSH descriptor ID is recorded as C565207[6].
- autosomal recessive nonsyndromic deafness 67's OMIM ID is recorded as 610265[7].
- autosomal recessive nonsyndromic deafness 67's Disease Ontology ID is recorded as DOID:0110518[8].
- autosomal recessive nonsyndromic deafness 67's genetic association is recorded as LHFPL5[9].
- autosomal recessive nonsyndromic deafness 67's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110518[10].
- autosomal recessive nonsyndromic deafness 67's exact match is recorded as http://identifiers.org/doid/DOID:0110518[11].
- autosomal recessive nonsyndromic deafness 67's UMLS CUI is recorded as C1853223[12].
- autosomal recessive nonsyndromic deafness 67's ICD-10-CM is recorded as H90.3[13].
- autosomal recessive nonsyndromic deafness 67's on focus list of Wikimedia project is recorded as WikiProject Medicine[14].
- autosomal recessive nonsyndromic deafness 67's Mondo ID is recorded as MONDO_0012460[15].
- autosomal recessive nonsyndromic deafness 67's UniProt disease ID is recorded as DI-02067[16].