retinitis pigmentosa 7
retinitis pigmentosa that has material basis in mutation in the PRPH2 gene on chromosome 6p21
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retinitis pigmentosa 7
Summary
retinitis pigmentosa 7 is a rare disease[1].
Key Facts
- retinitis pigmentosa 7's instance of is recorded as rare disease[2].
- retinitis pigmentosa 7's instance of is recorded as class of disease[3].
- retinitis pigmentosa 7 is a type of retinitis pigmentosa[4].
- retinitis pigmentosa 7 is a type of genetic disease[5].
- retinitis pigmentosa 7 is a type of autosomal recessive disease[6].
- retinitis pigmentosa 7 is a type of digenic disease[7].
- retinitis pigmentosa 7 is a type of autosomal dominant disease[8].
- retinitis pigmentosa 7's genetic association is recorded as ROM1[9].
- retinitis pigmentosa 7's genetic association is recorded as PRPH2[10].
- retinitis pigmentosa 7's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110383[11].
- retinitis pigmentosa 7's exact match is recorded as http://identifiers.org/doid/DOID:0110383[12].
- retinitis pigmentosa 7's on focus list of Wikimedia project is recorded as WikiProject Medicine[13].