autosomal recessive nonsyndromic deafness 35
autosomal recessive nonsyndromic deafness that is characterized severe to profound hearing loss and has material basis in mutation in the ESRRB gene on chromosome 14q24
Press Enter · cited answer in seconds
0 sources
autosomal recessive nonsyndromic deafness 35
Summary
autosomal recessive nonsyndromic deafness 35 is a head and neck disease[1].
Key Facts
- autosomal recessive nonsyndromic deafness 35's instance of is recorded as head and neck disease[2].
- autosomal recessive nonsyndromic deafness 35's instance of is recorded as rare disease[3].
- autosomal recessive nonsyndromic deafness 35's instance of is recorded as class of disease[4].
- autosomal recessive nonsyndromic deafness 35's subclass of is recorded as autosomal recessive nonsyndromic deafness[5].
- autosomal recessive nonsyndromic deafness 35's MeSH descriptor ID is recorded as C563908[6].
- autosomal recessive nonsyndromic deafness 35's OMIM ID is recorded as 608565[7].
- autosomal recessive nonsyndromic deafness 35's Disease Ontology ID is recorded as DOID:0110493[8].
- autosomal recessive nonsyndromic deafness 35's genetic association is recorded as ESRRB[9].
- autosomal recessive nonsyndromic deafness 35's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110493[10].
- autosomal recessive nonsyndromic deafness 35's exact match is recorded as http://identifiers.org/doid/DOID:0110493[11].
- autosomal recessive nonsyndromic deafness 35's UMLS CUI is recorded as C1837857[12].
- autosomal recessive nonsyndromic deafness 35's ICD-10-CM is recorded as H90.3[13].
- autosomal recessive nonsyndromic deafness 35's on focus list of Wikimedia project is recorded as WikiProject Medicine[14].
- autosomal recessive nonsyndromic deafness 35's Mondo ID is recorded as MONDO_0012060[15].
- autosomal recessive nonsyndromic deafness 35's UniProt disease ID is recorded as DI-00872[16].