retinitis pigmentosa 30
retinitis pigmentosa that has material basis in mutation in the FSCN2 gene on chromosome 17q25
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Summary
retinitis pigmentosa 30 is a rare disease[1].
Key Facts
- retinitis pigmentosa 30's instance of is recorded as rare disease[2].
- retinitis pigmentosa 30's instance of is recorded as class of disease[3].
- retinitis pigmentosa 30's subclass of is recorded as retinitis pigmentosa[4].
- retinitis pigmentosa 30's subclass of is recorded as genetic disease[5].
- retinitis pigmentosa 30's OMIM ID is recorded as 607921[6].
- retinitis pigmentosa 30's Disease Ontology ID is recorded as DOID:0110406[7].
- retinitis pigmentosa 30's genetic association is recorded as FSCN2[8].
- retinitis pigmentosa 30's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110406[9].
- retinitis pigmentosa 30's exact match is recorded as http://identifiers.org/doid/DOID:0110406[10].
- retinitis pigmentosa 30's UMLS CUI is recorded as C1842816[11].
- retinitis pigmentosa 30's ICD-10-CM is recorded as H35.5[12].
- retinitis pigmentosa 30's on focus list of Wikimedia project is recorded as WikiProject Medicine[13].
- retinitis pigmentosa 30's Mondo ID is recorded as MONDO_0011935[14].
- retinitis pigmentosa 30's UniProt disease ID is recorded as DI-00990[15].