retinitis pigmentosa 55
retinitis pigmentosa that has material basis in mutation in the ARL6 gene on chromosome 3q11.2
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retinitis pigmentosa 55
Summary
retinitis pigmentosa 55 is a rare disease[1].
Key Facts
- retinitis pigmentosa 55's instance of is recorded as rare disease[2].
- retinitis pigmentosa 55's instance of is recorded as class of disease[3].
- retinitis pigmentosa 55's subclass of is recorded as retinitis pigmentosa[4].
- retinitis pigmentosa 55's subclass of is recorded as genetic disease[5].
- retinitis pigmentosa 55's OMIM ID is recorded as 613575[6].
- retinitis pigmentosa 55's Disease Ontology ID is recorded as DOID:0110370[7].
- retinitis pigmentosa 55's genetic association is recorded as ARL6[8].
- retinitis pigmentosa 55's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110370[9].
- retinitis pigmentosa 55's exact match is recorded as http://identifiers.org/doid/DOID:0110370[10].
- retinitis pigmentosa 55's UMLS CUI is recorded as C3150808[11].
- retinitis pigmentosa 55's ICD-10-CM is recorded as H35.5[12].
- retinitis pigmentosa 55's on focus list of Wikimedia project is recorded as WikiProject Medicine[13].
- retinitis pigmentosa 55's Mondo ID is recorded as MONDO_0013312[14].
- retinitis pigmentosa 55's UniProt disease ID is recorded as DI-02896[15].