retinitis pigmentosa 68
retinitis pigmentosa that has material basis in mutation in the SLC7A14 gene on chromosome 3q26
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Summary
retinitis pigmentosa 68 is a rare disease[1].
Key Facts
- retinitis pigmentosa 68's instance of is recorded as rare disease[2].
- retinitis pigmentosa 68's instance of is recorded as class of disease[3].
- retinitis pigmentosa 68's subclass of is recorded as retinitis pigmentosa[4].
- retinitis pigmentosa 68's subclass of is recorded as genetic disease[5].
- retinitis pigmentosa 68's OMIM ID is recorded as 615725[6].
- retinitis pigmentosa 68's Disease Ontology ID is recorded as DOID:0110374[7].
- retinitis pigmentosa 68's genetic association is recorded as SLC7A14[8].
- retinitis pigmentosa 68's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110374[9].
- retinitis pigmentosa 68's exact match is recorded as http://identifiers.org/doid/DOID:0110374[10].
- retinitis pigmentosa 68's UMLS CUI is recorded as C3810380[11].
- retinitis pigmentosa 68's ICD-10-CM is recorded as H35.5[12].
- retinitis pigmentosa 68's on focus list of Wikimedia project is recorded as WikiProject Medicine[13].
- retinitis pigmentosa 68's Mondo ID is recorded as MONDO_0014323[14].
- retinitis pigmentosa 68's UniProt disease ID is recorded as DI-04064[15].