retinitis pigmentosa 56
retinitis pigmentosa that has material basis in mutation in the IMPG2 gene on chromosome 3q12.3
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Summary
retinitis pigmentosa 56 is a rare disease[1].
Key Facts
- retinitis pigmentosa 56's instance of is recorded as rare disease[2].
- retinitis pigmentosa 56's instance of is recorded as class of disease[3].
- retinitis pigmentosa 56 is a type of retinitis pigmentosa[4].
- retinitis pigmentosa 56 is a type of genetic disease[5].
- retinitis pigmentosa 56 is a type of autosomal recessive disease[6].
- retinitis pigmentosa 56's genetic association is recorded as IMPG2[7].
- retinitis pigmentosa 56's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110371[8].
- retinitis pigmentosa 56's exact match is recorded as http://identifiers.org/doid/DOID:0110371[9].
- retinitis pigmentosa 56's on focus list of Wikimedia project is recorded as WikiProject Medicine[10].