autosomal recessive nonsyndromic deafness 39
autosomal recessive nonsyndromic deafness that is characterized by prelingual onset with severe to profound, downsloping hearing loss and has material basis in mutation in the HGF gene on chromosome 7q21
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autosomal recessive nonsyndromic deafness 39
Summary
autosomal recessive nonsyndromic deafness 39 is a rare disease[1].
Key Facts
- autosomal recessive nonsyndromic deafness 39's instance of is recorded as rare disease[2].
- autosomal recessive nonsyndromic deafness 39's instance of is recorded as class of disease[3].
- autosomal recessive nonsyndromic deafness 39's subclass of is recorded as autosomal recessive nonsyndromic deafness[4].
- autosomal recessive nonsyndromic deafness 39's MeSH descriptor ID is recorded as C564265[5].
- autosomal recessive nonsyndromic deafness 39's OMIM ID is recorded as 608265[6].
- autosomal recessive nonsyndromic deafness 39's Disease Ontology ID is recorded as DOID:0110497[7].
- autosomal recessive nonsyndromic deafness 39's NCI Thesaurus ID is recorded as C129874[8].
- autosomal recessive nonsyndromic deafness 39's genetic association is recorded as HGF[9].
- autosomal recessive nonsyndromic deafness 39's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110497[10].
- autosomal recessive nonsyndromic deafness 39's exact match is recorded as http://identifiers.org/doid/DOID:0110497[11].
- autosomal recessive nonsyndromic deafness 39's UMLS CUI is recorded as C1842342[12].
- autosomal recessive nonsyndromic deafness 39's ICD-10-CM is recorded as H90.3[13].
- autosomal recessive nonsyndromic deafness 39's on focus list of Wikimedia project is recorded as WikiProject Medicine[14].
- autosomal recessive nonsyndromic deafness 39's Mondo ID is recorded as MONDO_0012003[15].
- autosomal recessive nonsyndromic deafness 39's UniProt disease ID is recorded as DI-02477[16].