retinitis pigmentosa 49
human disease
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retinitis pigmentosa 49
Summary
retinitis pigmentosa 49 is a rare disease[1].
Key Facts
- retinitis pigmentosa 49's instance of is recorded as rare disease[2].
- retinitis pigmentosa 49's instance of is recorded as class of disease[3].
- retinitis pigmentosa 49's subclass of is recorded as retinitis pigmentosa[4].
- retinitis pigmentosa 49's subclass of is recorded as genetic disease[5].
- retinitis pigmentosa 49's OMIM ID is recorded as 613756[6].
- retinitis pigmentosa 49's Disease Ontology ID is recorded as DOID:0110377[7].
- retinitis pigmentosa 49's genetic association is recorded as CNGA1[8].
- retinitis pigmentosa 49's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110377[9].
- retinitis pigmentosa 49's exact match is recorded as http://identifiers.org/doid/DOID:0110377[10].
- retinitis pigmentosa 49's UMLS CUI is recorded as C3151059[11].
- retinitis pigmentosa 49's ICD-10-CM is recorded as H35.5[12].
- retinitis pigmentosa 49's on focus list of Wikimedia project is recorded as WikiProject Medicine[13].
- retinitis pigmentosa 49's Mondo ID is recorded as MONDO_0013405[14].
- retinitis pigmentosa 49's UniProt disease ID is recorded as DI-03002[15].