retinitis pigmentosa 67
retinitis pigmentosa that has material basis in mutation in the NEK2 gene on chromosome 1q32
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retinitis pigmentosa 67
Summary
retinitis pigmentosa 67 is a rare disease[1].
Key Facts
- retinitis pigmentosa 67's instance of is recorded as rare disease[2].
- retinitis pigmentosa 67's instance of is recorded as class of disease[3].
- retinitis pigmentosa 67's subclass of is recorded as retinitis pigmentosa[4].
- retinitis pigmentosa 67's subclass of is recorded as genetic disease[5].
- retinitis pigmentosa 67's OMIM ID is recorded as 615565[6].
- retinitis pigmentosa 67's Disease Ontology ID is recorded as DOID:0110359[7].
- retinitis pigmentosa 67's genetic association is recorded as NEK2[8].
- retinitis pigmentosa 67's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110359[9].
- retinitis pigmentosa 67's exact match is recorded as http://identifiers.org/doid/DOID:0110359[10].
- retinitis pigmentosa 67's UMLS CUI is recorded as C3809954[11].
- retinitis pigmentosa 67's ICD-10-CM is recorded as H35.5[12].
- retinitis pigmentosa 67's on focus list of Wikimedia project is recorded as WikiProject Medicine[13].
- retinitis pigmentosa 67's Mondo ID is recorded as MONDO_0014256[14].
- retinitis pigmentosa 67's UniProt disease ID is recorded as DI-03990[15].