autosomal recessive nonsyndromic deafness 21
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 TECTA gene on chromosome 11q23.3
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autosomal recessive nonsyndromic deafness 21
Summary
autosomal recessive nonsyndromic deafness 21 is a rare disease[1].
Key Facts
- autosomal recessive nonsyndromic deafness 21's instance of is recorded as rare disease[2].
- autosomal recessive nonsyndromic deafness 21's instance of is recorded as class of disease[3].
- autosomal recessive nonsyndromic deafness 21's subclass of is recorded as autosomal recessive nonsyndromic deafness[4].
- autosomal recessive nonsyndromic deafness 21's MeSH descriptor ID is recorded as C566353[5].
- autosomal recessive nonsyndromic deafness 21's OMIM ID is recorded as 603629[6].
- autosomal recessive nonsyndromic deafness 21's Disease Ontology ID is recorded as DOID:0110479[7].
- autosomal recessive nonsyndromic deafness 21's genetic association is recorded as TECTA[8].
- autosomal recessive nonsyndromic deafness 21's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110479[9].
- autosomal recessive nonsyndromic deafness 21's exact match is recorded as http://identifiers.org/doid/DOID:0110479[10].
- autosomal recessive nonsyndromic deafness 21's UMLS CUI is recorded as C1863655[11].
- autosomal recessive nonsyndromic deafness 21's ICD-10-CM is recorded as H90.3[12].
- autosomal recessive nonsyndromic deafness 21's on focus list of Wikimedia project is recorded as WikiProject Medicine[13].
- autosomal recessive nonsyndromic deafness 21's Mondo ID is recorded as MONDO_0011351[14].
- autosomal recessive nonsyndromic deafness 21's UniProt disease ID is recorded as DI-00865[15].