autosomal recessive nonsyndromic deafness 25
autosomal recessive nonsyndromic deafness that is characterized by prelingual onset with moderate to profound, progressive hearing loss and has material basis in mutation in the GRXCR1 gene on chromosome 4p13
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autosomal recessive nonsyndromic deafness 25
Summary
autosomal recessive nonsyndromic deafness 25 is a rare disease[1].
Key Facts
- autosomal recessive nonsyndromic deafness 25's instance of is recorded as rare disease[2].
- autosomal recessive nonsyndromic deafness 25's instance of is recorded as class of disease[3].
- autosomal recessive nonsyndromic deafness 25's subclass of is recorded as autosomal recessive nonsyndromic deafness[4].
- autosomal recessive nonsyndromic deafness 25's OMIM ID is recorded as 613285[5].
- autosomal recessive nonsyndromic deafness 25's Disease Ontology ID is recorded as DOID:0110483[6].
- autosomal recessive nonsyndromic deafness 25's genetic association is recorded as GRXCR1[7].
- autosomal recessive nonsyndromic deafness 25's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110483[8].
- autosomal recessive nonsyndromic deafness 25's exact match is recorded as http://identifiers.org/doid/DOID:0110483[9].
- autosomal recessive nonsyndromic deafness 25's UMLS CUI is recorded as C1414017[10].
- autosomal recessive nonsyndromic deafness 25's ICD-10-CM is recorded as H90.3[11].
- autosomal recessive nonsyndromic deafness 25's on focus list of Wikimedia project is recorded as WikiProject Medicine[12].
- autosomal recessive nonsyndromic deafness 25's Mondo ID is recorded as MONDO_0013210[13].
- autosomal recessive nonsyndromic deafness 25's UniProt disease ID is recorded as DI-02537[14].