retinitis pigmentosa 36
retinitis pigmentosa that has material basis in mutation in the PRCD gene on chromosome 17q25
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retinitis pigmentosa 36
Summary
retinitis pigmentosa 36 is a rare disease[1].
Key Facts
- retinitis pigmentosa 36's instance of is recorded as rare disease[2].
- retinitis pigmentosa 36's instance of is recorded as class of disease[3].
- retinitis pigmentosa 36's subclass of is recorded as retinitis pigmentosa[4].
- retinitis pigmentosa 36's subclass of is recorded as genetic disease[5].
- retinitis pigmentosa 36's MeSH descriptor ID is recorded as C566431[6].
- retinitis pigmentosa 36's OMIM ID is recorded as 610599[7].
- retinitis pigmentosa 36's Disease Ontology ID is recorded as DOID:0110405[8].
- retinitis pigmentosa 36's genetic association is recorded as PRCD[9].
- retinitis pigmentosa 36's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110405[10].
- retinitis pigmentosa 36's exact match is recorded as http://identifiers.org/doid/DOID:0110405[11].
- retinitis pigmentosa 36's UMLS CUI is recorded as C1864621[12].
- retinitis pigmentosa 36's ICD-10-CM is recorded as H35.5[13].
- retinitis pigmentosa 36's GARD rare disease ID is recorded as 10403[14].
- retinitis pigmentosa 36's on focus list of Wikimedia project is recorded as WikiProject Medicine[15].
- retinitis pigmentosa 36's Mondo ID is recorded as MONDO_0012523[16].
- retinitis pigmentosa 36's UniProt disease ID is recorded as DI-02263[17].