autosomal recessive nonsyndromic deafness 68
autosomal recessive nonsyndromic deafness that has material basis in mutation in the S1PR2 gene on chromosome 19p13
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autosomal recessive nonsyndromic deafness 68
Summary
autosomal recessive nonsyndromic deafness 68 is a rare disease[1].
Key Facts
- autosomal recessive nonsyndromic deafness 68's instance of is recorded as rare disease[2].
- autosomal recessive nonsyndromic deafness 68's instance of is recorded as class of disease[3].
- autosomal recessive nonsyndromic deafness 68's subclass of is recorded as autosomal recessive nonsyndromic deafness[4].
- autosomal recessive nonsyndromic deafness 68's MeSH descriptor ID is recorded as C563669[5].
- autosomal recessive nonsyndromic deafness 68's OMIM ID is recorded as 610419[6].
- autosomal recessive nonsyndromic deafness 68's Disease Ontology ID is recorded as DOID:0110519[7].
- autosomal recessive nonsyndromic deafness 68's genetic association is recorded as S1PR2[8].
- autosomal recessive nonsyndromic deafness 68's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110519[9].
- autosomal recessive nonsyndromic deafness 68's exact match is recorded as http://identifiers.org/doid/DOID:0110519[10].
- autosomal recessive nonsyndromic deafness 68's UMLS CUI is recorded as C1835854[11].
- autosomal recessive nonsyndromic deafness 68's ICD-10-CM is recorded as H90.3[12].
- autosomal recessive nonsyndromic deafness 68's on focus list of Wikimedia project is recorded as WikiProject Medicine[13].
- autosomal recessive nonsyndromic deafness 68's Mondo ID is recorded as MONDO_0012485[14].
- autosomal recessive nonsyndromic deafness 68's UniProt disease ID is recorded as DI-04685[15].