retinitis pigmentosa 66
retinitis pigmentosa that has material basis in mutation in the RBP3 gene on chromosome 10q11
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Summary
retinitis pigmentosa 66 is a rare disease[1].
Key Facts
- retinitis pigmentosa 66's instance of is recorded as rare disease[2].
- retinitis pigmentosa 66's instance of is recorded as class of disease[3].
- retinitis pigmentosa 66's subclass of is recorded as retinitis pigmentosa[4].
- retinitis pigmentosa 66's subclass of is recorded as genetic disease[5].
- retinitis pigmentosa 66's OMIM ID is recorded as 615233[6].
- retinitis pigmentosa 66's Disease Ontology ID is recorded as DOID:0110393[7].
- retinitis pigmentosa 66's genetic association is recorded as RBP3[8].
- retinitis pigmentosa 66's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110393[9].
- retinitis pigmentosa 66's exact match is recorded as http://identifiers.org/doid/DOID:0110393[10].
- retinitis pigmentosa 66's UMLS CUI is recorded as C3715216[11].
- retinitis pigmentosa 66's ICD-10-CM is recorded as H35.5[12].
- retinitis pigmentosa 66's on focus list of Wikimedia project is recorded as WikiProject Medicine[13].
- retinitis pigmentosa 66's Mondo ID is recorded as MONDO_0014093[14].
- retinitis pigmentosa 66's UniProt disease ID is recorded as DI-03727[15].