Medical Subject Headings / 医学主题词表

Last uploaded: September 7, 2023
Preferred Name

Color Vision Defects

Synonyms

Blue Color Blindness

Definitions

Defects of color vision are mainly hereditary traits but can be secondary to acquired or developmental abnormalities in the CONES (RETINA). Severity of hereditary defects of color vision depends on the degree of mutation of the ROD OPSINS genes (on X CHROMOSOME and CHROMOSOME 3) that code the photopigments for red, green and blue.

ID

http://purl.bioontology.org/ontology/MESH/D003117

altLabel

Blue Color Blindness

Color Blindness, Red

Monochromatopsia

Color Blindness, Red-Green

Blindness, Color

Deficiency, Color Vision

Green Color Blindness

Deutan Defect

Color Blindness, Acquired

Tritan Defect

Color Vision Deficiencies

Vision Deficiency, Color

Vision Defect, Color

Defects, Color Vision

Defect, Color Vision

Color Vision Defect

Protan Defect

Color Blindness, Red Green

Color Blindness

Inherited Color Blindness

Color Blindness, Green

Color Vision Deficiency

Defect, Deutan

Acquired Color Blindness

Achromatopsia

Vision Deficiencies, Color

Deficiencies, Color Vision

Color Blindness, Blue

Color Blindness, Inherited

Achromatopsias

Red Color Blindness

Red-Green Color Blindness

Vision Defects, Color

AQL

BL CF CI CL CN CO DG DH DI DT EC EH EM EN EP ET GE HI IM ME MI MO NU PA PC PP PS PX RH RT SU TH UR VE VI

cui

C0155015

C0009398

C0155018

C0751042

C0152200

C0751043

C0239777

C0155017

C0242225

C0155016

DC

1

definition

Defects of color vision are mainly hereditary traits but can be secondary to acquired or developmental abnormalities in the CONES (RETINA). Severity of hereditary defects of color vision depends on the degree of mutation of the ROD OPSINS genes (on X CHROMOSOME and CHROMOSOME 3) that code the photopigments for red, green and blue.

Severely deficient color perception, typically with monochromacy and reduced visual acuity. The atypical form can include normal visual acuity with pseudomonochromacy.

DX

19900101

FX

D012164

D017949

HN

90; was COLOR BLINDNESS 1963-89

Inverse of AQ

http://purl.bioontology.org/ontology/MESH/Q000401

http://purl.bioontology.org/ontology/MESH/Q000150

http://purl.bioontology.org/ontology/MESH/Q000188

http://purl.bioontology.org/ontology/MESH/Q000517

http://purl.bioontology.org/ontology/MESH/Q000201

http://purl.bioontology.org/ontology/MESH/Q000145

http://purl.bioontology.org/ontology/MESH/Q000503

http://purl.bioontology.org/ontology/MESH/Q000453

http://purl.bioontology.org/ontology/MESH/Q000208

http://purl.bioontology.org/ontology/MESH/Q000134

http://purl.bioontology.org/ontology/MESH/Q000821

http://purl.bioontology.org/ontology/MESH/Q000382

http://purl.bioontology.org/ontology/MESH/Q000601

http://purl.bioontology.org/ontology/MESH/Q000235

http://purl.bioontology.org/ontology/MESH/Q000523

http://purl.bioontology.org/ontology/MESH/Q000276

http://purl.bioontology.org/ontology/MESH/Q000191

http://purl.bioontology.org/ontology/MESH/Q000652

http://purl.bioontology.org/ontology/MESH/Q000662

http://purl.bioontology.org/ontology/MESH/Q000151

http://purl.bioontology.org/ontology/MESH/Q000628

http://purl.bioontology.org/ontology/MESH/Q000196

http://purl.bioontology.org/ontology/MESH/Q000534

http://purl.bioontology.org/ontology/MESH/Q000266

http://purl.bioontology.org/ontology/MESH/Q000532

http://purl.bioontology.org/ontology/MESH/Q000139

http://purl.bioontology.org/ontology/MESH/Q000378

http://purl.bioontology.org/ontology/MESH/Q000175

http://purl.bioontology.org/ontology/MESH/Q000000981

http://purl.bioontology.org/ontology/MESH/Q000097

http://purl.bioontology.org/ontology/MESH/Q000473

http://purl.bioontology.org/ontology/MESH/Q000451

http://purl.bioontology.org/ontology/MESH/Q000209

http://purl.bioontology.org/ontology/MESH/Q000178

http://purl.bioontology.org/ontology/MESH/Q000469

Inverse of RO

http://purl.bioontology.org/ontology/MESH/D017949

http://purl.bioontology.org/ontology/MESH/D003118

http://purl.bioontology.org/ontology/MESH/D012164

Machine permutation

90; was COLOR BLINDNESS 1963-89

Mapped from

http://purl.bioontology.org/ontology/MESH/C536129

http://purl.bioontology.org/ontology/MESH/C564440

http://purl.bioontology.org/ontology/MESH/C536128

http://purl.bioontology.org/ontology/MESH/C536238

http://purl.bioontology.org/ontology/MESH/C538165

http://purl.bioontology.org/ontology/MESH/C564206

http://purl.bioontology.org/ontology/MESH/C567759

http://purl.bioontology.org/ontology/MESH/C536021

MDA

19990101

MMR

20180629

MN

C11.270.151.500

C11.966.256

C10.597.751.941.256

C23.888.592.763.941.256

notation

D003117

OL

use COLOR VISION DEFECTS to search COLOR BLINDNESS 1966-89

prefLabel

Color Vision Defects

TERMUI

T371312

T371304

T371310

T371309

T009095

T371303

T371302

T371308

T841142

T371306

T371311

T009096

T371307

T371305

TH

NLM (1990)

NLM (2000)

NLM (1966)

NLM (2014)

GHR (2014)

tui

T047

subClassOf

http://purl.bioontology.org/ontology/MESH/D000077765

http://purl.bioontology.org/ontology/MESH/D014786

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http://purl.bioontology.org/ontology/ICD10CM/H53.52 International Classification of Diseases, Version 10 - Clinical Modification / 国际疾病分类,第10版-临床修改 CUI
http://purl.bioontology.org/ontology/MEDLINEPLUS/C0242225 MedlinePlus Health Topics / MedlinePlus网站健康主题 CUI
http://purl.bmicc.cn/ontology/ICD10CN/H53.5 《国际疾病分类》第10版中文版 / International Classification of Diseases, 10th Edition, China CUI
http://purl.bioontology.org/ontology/OMIM/MTHU023559 Online Mendelian Inheritance in Man / 在线人类孟德尔遗传数据库 CUI
http://purl.bioontology.org/ontology/OMIM/MTHU065090 Online Mendelian Inheritance in Man / 在线人类孟德尔遗传数据库 CUI
http://purl.bioontology.org/ontology/ICD10CM/H53.55 International Classification of Diseases, Version 10 - Clinical Modification / 国际疾病分类,第10版-临床修改 CUI
http://purl.bioontology.org/ontology/LNC/LA32588-8 Logical Observation Identifier Names and Codes / 逻辑观察标识符名称和代码 CUI
http://purl.bioontology.org/ontology/ICD10CM/H53.5 International Classification of Diseases, Version 10 - Clinical Modification / 国际疾病分类,第10版-临床修改 CUI
http://purl.bioontology.org/ontology/ICD10CM/H53.5 International Classification of Diseases, Version 10 - Clinical Modification / 国际疾病分类,第10版-临床修改 CUI
http://purl.bioontology.org/ontology/OMIM/MTHU006100 Online Mendelian Inheritance in Man / 在线人类孟德尔遗传数据库 CUI
http://purl.bioontology.org/ontology/OMIM/MTHU006100 Online Mendelian Inheritance in Man / 在线人类孟德尔遗传数据库 LOOM
http://purl.bioontology.org/ontology/LNC/LA32593-8 Logical Observation Identifier Names and Codes / 逻辑观察标识符名称和代码 CUI
http://purl.bioontology.org/ontology/OMIM/303800 Online Mendelian Inheritance in Man / 在线人类孟德尔遗传数据库 CUI
http://purl.bioontology.org/ontology/OMIM/MTHU016525 Online Mendelian Inheritance in Man / 在线人类孟德尔遗传数据库 CUI
http://purl.bioontology.org/ontology/LNC/LP428978-3 Logical Observation Identifier Names and Codes / 逻辑观察标识符名称和代码 CUI
http://purl.bioontology.org/ontology/LNC/MTHU067226 Logical Observation Identifier Names and Codes / 逻辑观察标识符名称和代码 CUI
http://purl.bioontology.org/ontology/OMIM/190900 Online Mendelian Inheritance in Man / 在线人类孟德尔遗传数据库 CUI
http://purl.bioontology.org/ontology/OMIM/613522 Online Mendelian Inheritance in Man / 在线人类孟德尔遗传数据库 CUI
http://purl.bioontology.org/ontology/OMIM/MTHU070750 Online Mendelian Inheritance in Man / 在线人类孟德尔遗传数据库 CUI
http://purl.bioontology.org/ontology/OMIM/MTHU073630 Online Mendelian Inheritance in Man / 在线人类孟德尔遗传数据库 CUI
http://purl.bioontology.org/ontology/OMIM/MTHU023012 Online Mendelian Inheritance in Man / 在线人类孟德尔遗传数据库 CUI
http://purl.bioontology.org/ontology/OMIM/MTHU010446 Online Mendelian Inheritance in Man / 在线人类孟德尔遗传数据库 CUI
http://purl.bioontology.org/ontology/ICD10/H53.5 International Classification of Diseases, Version 10 / 《国际疾病分类》第10版 CUI
http://purl.bioontology.org/ontology/OMIM/MTHU000023 Online Mendelian Inheritance in Man / 在线人类孟德尔遗传数据库 CUI
http://purl.bioontology.org/ontology/ICD10CM/H53.50 International Classification of Diseases, Version 10 - Clinical Modification / 国际疾病分类,第10版-临床修改 CUI
http://purl.bioontology.org/ontology/OMIM/MTHU016524 Online Mendelian Inheritance in Man / 在线人类孟德尔遗传数据库 CUI
http://purl.bioontology.org/ontology/ICD10CM/H53.51 International Classification of Diseases, Version 10 - Clinical Modification / 国际疾病分类,第10版-临床修改 CUI