SHMARQL

achromatopsia 5

<http://www.wikidata.org/entity/Q93950751>

human disease
rdfs:label
"achromatopsia 5"@en
skos:altLabel "ACHM5"@en
"COD4"@en
"cone dystrophy 4"@en
schema:description
"human disease"@en
schema:dateModified "2026-07-04T14:11:34+00:00"^^xsd:dateTime
schema:version 2513825461
wikibase:identifiers 3
wikibase:sitelinks 0
wikibase:statements 8
p:P11430 wd:statement/Q93950751-791bccd1-4578-a857-9a06-fc3a2f0f432f
p:P1748 wd:statement/Q93950751-d4c3c80f-4ac1-1141-8f47-400ba8072be4
p:P2293 wd:statement/Q93950751-8b450a4e-4e2a-84b5-9f7a-152baf92f993
p:P279 wd:statement/Q93950751-445b4553-4736-0806-8b95-cb2caaed2fbc
p:P31 wd:statement/Q93950751-37051028-4bcc-8276-d245-6e8b5b055a72
wd:statement/Q93950751-4e502cbd-47a4-6821-c188-2afba5e5c203
p:P492 wd:statement/Q93950751-027a1827-407a-b7fa-c009-210cb85dd1e8
p:P5270 wd:statement/Q93950751-7893DB42-2032-470A-B242-709A78258185
p:direct-normalized/P5270 <http://purl.obolibrary.org/obo/MONDO_0013129>
wdt:P11430 "DI-05080"
wdt:P1748 "C164226"
wdt:P2293 PDE6C
wdt:P279 achromatopsia
wdt:P31 type of disease
rare disease
wdt:P492 "613093"
wdt:P5270 "MONDO_0013129"
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data from SPARQL profile: Wikidata