achromatopsia

human illness, a type of color blindness
rdfs:label
"achromatopsia"@en
skos:altLabel
"ACHM"@en
"Complete or incomplete color blindness"@en
"Pingelapese blindness"@en
"Rod monochromacy"@en
"Rod monochromatism"@en
"complete achromatopsia"@en
"complete color blindness"@en
"monochromacy"@en
"monochromatism"@en
"rod monochromacy"@en
"rod monochromatism"@en
"total color blindness"@en
"typical achromatopsia"@en
schema:description
"human illness, a type of color blindness"@en
schema:dateModified "2026-11-13T15:23:42+00:00"^^xsd:dateTime
schema:version 2568745657
wikibase:identifiers 27
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wikibase:sitelinks 23
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p:direct-normalized/P2163 <http://id.worldcat.org/fast/868530>
p:direct-normalized/P227 <https://d-nb.info/gnd/4242792-7>
p:direct-normalized/P244 <http://id.loc.gov/authorities/names/sh85028584>
p:direct-normalized/P5270 <http://purl.obolibrary.org/obo/MONDO_0018852>
p:direct-normalized/P6366 <https://makg.org/entity/2777906962>
p:direct-normalized/P665 <http://www.kegg.jp/entry/H00971>
p:direct-normalized/P699 <http://purl.obolibrary.org/obo/DOID_DOID:13911>
wdt:P10283 "C2777906962"
wdt:P11143 "Achromatopsia"
wdt:P1193 0.00005^^xsd:decimal
wdt:P1245 "1487538"
wdt:P1343 The Unified Medical Dictionary (Librairie du Liban, 2009)
wdt:P13591 "concept/22b88227-9595-4067-b54b-23e8fd83bac4"
wdt:P1417 "topic/achromatopsia"
wdt:P14914 "D49382"
wdt:P1550 "49382"
wdt:P1692 "368.54"
wdt:P1748 "C84528"
wdt:P1995 ophthalmology
wdt:P2163 "868530"
wdt:P227 "4242792-7"
wdt:P2293 CNGA3
OPN1MW
GNAT2
PDE6C
PDE6H
OPN1LW
RPGR
ATF6
CNGB3
wdt:P244 "sh85028584"
wdt:P279 monochromacy
wdt:P2841 neonatal onset
infantile onset
wdt:P2888 <http://identifiers.org/doid/DOID:13911>
<http://purl.obolibrary.org/obo/DOID_13911>
<http://www.orpha.net/ORDO/Orphanet_49382>
wdt:P2892 "C0152200"
wdt:P31 type of disease
rare disease
wdt:P3417 "Achromatopsia"
wdt:P373 "Achromatopsia"
wdt:P3841 "HP:0011516"
wdt:P4229 "H53.5"
"H53.51"
wdt:P4802 "110662"
wdt:P492 "303700"
wdt:P5008 WikiProject Medicine
wdt:P5082 "akromatopsi"
wdt:P5270 "MONDO_0018852"
wdt:P557 "83"
wdt:P6366 "2777906962"
wdt:P6532 Attenuation of retinal blood vessels
Abnormal macular morphology
Reduced visual acuity
Abnormal pupillary light reflex
Retinal pigment epithelial atrophy
myopia
hyperopia
central scotoma
photophobia
refractive error
wdt:P6611 "187726"
wdt:P665 "H00971"
wdt:P689 rod cell
wdt:P699 "DOID:13911"
wdt:P7464 "achromatopsia"
wdt:P780 amblyopia
nystagmus
photophobia
wdt:P7807 "266505357"
wdt:P8189 "987007284741605171"
wdt:P8313 "akromatopsi"
wdt:P8855 "845-22-028"
wdt:P949 "000664610"
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