autosomal recessive nonsyndromic deafness 30
autosomal recessive nonsyndromic deafness that is characterized by prelingual onset with severe to profound, stable hearing loss and has material basis in mutations in the MYO3A gene on chromosome 10p12.1
Press Enter · cited answer in seconds
0 sources
autosomal recessive nonsyndromic deafness 30
Summary
autosomal recessive nonsyndromic deafness 30 is a rare disease[1].
Key Facts
- autosomal recessive nonsyndromic deafness 30's instance of is recorded as rare disease[2].
- autosomal recessive nonsyndromic deafness 30's instance of is recorded as class of disease[3].
- autosomal recessive nonsyndromic deafness 30's subclass of is recorded as autosomal recessive nonsyndromic deafness[4].
- autosomal recessive nonsyndromic deafness 30's MeSH descriptor ID is recorded as C564624[5].
- autosomal recessive nonsyndromic deafness 30's OMIM ID is recorded as 607101[6].
- autosomal recessive nonsyndromic deafness 30's Disease Ontology ID is recorded as DOID:0110489[7].
- autosomal recessive nonsyndromic deafness 30's Orphanet ID is recorded as 90636[8].
- autosomal recessive nonsyndromic deafness 30's genetic association is recorded as MYO3A[9].
- autosomal recessive nonsyndromic deafness 30's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110489[10].
- autosomal recessive nonsyndromic deafness 30's exact match is recorded as http://identifiers.org/doid/DOID:0110489[11].
- autosomal recessive nonsyndromic deafness 30's UMLS CUI is recorded as C1846784[12].
- autosomal recessive nonsyndromic deafness 30's ICD-10-CM is recorded as H90.3[13].
- autosomal recessive nonsyndromic deafness 30's on focus list of Wikimedia project is recorded as WikiProject Medicine[14].
- autosomal recessive nonsyndromic deafness 30's Mondo ID is recorded as MONDO_0011774[15].
- autosomal recessive nonsyndromic deafness 30's UniProt disease ID is recorded as DI-00870[16].