retinitis pigmentosa 2
retinitis pigmentosa that has material basis in mutation in the RP2 gene on chromosome Xp11.3
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retinitis pigmentosa 2
Summary
retinitis pigmentosa 2 is a rare disease[1].
Key Facts
- retinitis pigmentosa 2's instance of is recorded as rare disease[2].
- retinitis pigmentosa 2's instance of is recorded as class of disease[3].
- retinitis pigmentosa 2's subclass of is recorded as retinitis pigmentosa[4].
- retinitis pigmentosa 2's subclass of is recorded as genetic disease[5].
- retinitis pigmentosa 2's MeSH descriptor ID is recorded as C567523[6].
- retinitis pigmentosa 2's OMIM ID is recorded as 312600[7].
- retinitis pigmentosa 2's Disease Ontology ID is recorded as DOID:0110415[8].
- retinitis pigmentosa 2's genetic association is recorded as RP2[9].
- retinitis pigmentosa 2's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110415[10].
- retinitis pigmentosa 2's exact match is recorded as http://identifiers.org/doid/DOID:0110415[11].
- retinitis pigmentosa 2's UMLS CUI is recorded as C2681923[12].
- retinitis pigmentosa 2's ICD-10-CM is recorded as H35.5[13].
- retinitis pigmentosa 2's GARD rare disease ID is recorded as 8360[14].
- retinitis pigmentosa 2's on focus list of Wikimedia project is recorded as WikiProject Medicine[15].
- retinitis pigmentosa 2's Mondo ID is recorded as MONDO_0010723[16].
- retinitis pigmentosa 2's UniProt disease ID is recorded as DI-00972[17].