cone dystrophy

inherited ocular disorder characterized by the loss of cone cells
rdfs:label
"cone dystrophy"@en
skos:altLabel
"Cone Dystrophy, Autosomal Dominant"@en
"RCD1"@en
"RETINAL CONE DYSTROPHY 1"@en
"RETINAL CONE DYSTROPHY 1; RCD1"@en
"Retinal Cone Degeneration"@en
"retinal cone dystrophy"@en
schema:description
"inherited ocular disorder characterized by the loss of cone cells"@en
schema:dateModified "2026-10-23T03:53:52+00:00"^^xsd:dateTime
schema:version 2559838805
wikibase:identifiers 19
wikibase:sitelinks 10
wikibase:statements 33
p:P11143 wd:statement/Q147270-90EF4CAA-AA26-4CFB-A3C5-51D7B0E0B7CB
p:P18 wd:statement/Q147270-d64552f6-4d02-fd23-8b27-52224ec6defc
p:P1995 wd:statement/Q147270-1653E96F-9EE5-4BA4-94E5-A2B77B71A6F7
p:P2293 wd:statement/Q147270-788F6D2E-0B68-4295-8CAA-6D9F7FA77420
wd:statement/Q147270-9DE15711-A77E-44C9-87B5-E8F314FEAF06
wd:statement/Q147270-D404D975-951B-4F82-B27B-D2D28712F6CF
wd:statement/Q147270-D9EC24E7-522E-437E-8E64-6BEAB7586AEA
p:P2581 wd:statement/Q147270-34E33EA0-2D4B-4736-9244-3274921CFDB8
p:P279 wd:statement/Q147270-08AB7EC8-B7E7-4D9E-96B3-5A851EA42143
p:P2888 wd:statement/Q147270-24466A79-8D0B-4EE7-82F0-D44DCB162A08
wd:statement/Q147270-58D4E919-0E3B-4521-890E-9629FBF0BE7A
wd:statement/Q147270-E21854C1-1C66-436F-A93B-348C6C5A5CCD
p:P2892 wd:statement/Q147270-7EC93D8A-06F9-4F1F-859D-0D77A13C8115
wd:statement/Q147270-D45A61BC-E615-4006-B0E9-A329C765AF89
p:P31 wd:statement/Q147270-1E2CC604-F653-4E3B-B097-62AC5B824E72
wd:statement/Q147270-938CBADC-07FC-4CB5-B249-20D1F4E19141
p:P373 wd:statement/Q147270-DC41A6A3-BCFA-492F-A750-456B919B5FD9
p:P3841 wd:statement/Q147270-725F549F-DDF5-405F-A8F2-327DBBC577FE
p:P4233 wd:statement/Q147270-8d8bc62a-48c2-31b4-7ff9-acebe0c9de3a
p:P4317 wd:statement/Q147270-30C1A8FB-3F17-4DB8-8112-36ED50E09DB7
p:P486 wd:statement/Q147270-57849ADE-D3C8-4401-AA15-E4D5DFC221C6
p:P492 wd:statement/Q147270-13690355-8758-4D22-957E-C484488C3E33
wd:statement/Q147270-44D505ED-332A-4C65-9467-39149A712280
wd:statement/Q147270-59FC016E-6C62-4E5A-B3BB-0952DDC3A3E0
wd:statement/Q147270-B6830DFB-6199-410C-B9B7-AAD0F14CA6DF
wd:statement/Q147270-BE58870B-6570-4EB0-BF75-2F8915E84F37
p:P494 wd:statement/q147270-65ED243B-5673-49BC-ABE4-5103736CE1E1
p:P5008 wd:statement/Q147270-049524CD-7233-46D3-BEDC-9F341089FB85
p:P5270 wd:statement/Q147270-4A75C8D1-11A4-4DBB-85C4-C123D0306705
p:P6366 wd:statement/Q147270-79683A93-B6BC-4A3A-A9C7-52041686AC9D
p:P672 wd:statement/Q147270-a34ec011-4b28-3a7b-9b8c-83cbfa35caf3
wd:statement/Q147270-ae2a78df-4109-d0ea-3c25-b9662a64ad7d
p:P699 wd:statement/Q147270-55E88A87-445C-465F-99AD-70213F374A3D
p:direct-normalized/P2581 <http://babelnet.org/rdf/s01749600n>
p:direct-normalized/P486 <http://id.nlm.nih.gov/mesh/D000077765>
p:direct-normalized/P5270 <http://purl.obolibrary.org/obo/MONDO_0008374>
p:direct-normalized/P6366 <https://makg.org/entity/2778758327>
p:direct-normalized/P672 <http://id.nlm.nih.gov/mesh/C11.270.151>
<http://id.nlm.nih.gov/mesh/C11.768.216>
p:direct-normalized/P699 <http://purl.obolibrary.org/obo/DOID_DOID:0050795>
wdt:P11143 "Cone dystrophy"
wdt:P18 <http://commons.wikimedia.org/wiki/Special:FilePath/Fundus%20of%20a%20patient%20with%20cone%20rod%20dystrophy.png>
wdt:P1995 ophthalmology
wdt:P2293 PDE6C
PDE6H
CACNA2D4
KCNV2
wdt:P2581 "01749600n"
wdt:P279 retinal disease
wdt:P2888 <http://identifiers.org/doid/DOID:0050795>
<http://purl.obolibrary.org/obo/DOID_0050795>
<http://www.orpha.net/ORDO/Orphanet_1871>
wdt:P2892 "C0730290"
"C1867326"
wdt:P31 type of disease
rare disease
wdt:P373 "Cone dystrophy"
wdt:P3841 "HP:0008020"
wdt:P4233 "cone-dystrophy"
wdt:P4317 "10790"
wdt:P486 "D000077765"
wdt:P492 "180020"
"610024"
"610356"
"610478"
"613093"
wdt:P494 "H35.5"
wdt:P5008 WikiProject Medicine
wdt:P5270 "MONDO_0008374"
wdt:P6366 "2778758327"
wdt:P672 "C11.270.151"
"C11.768.216"
wdt:P699 "DOID:0050795"
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