MCID: RDC001
MIFTS: 21

Red Color Blindness malady

Summaries for Red Color Blindness

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32MalaCards
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MalaCards: Red Color Blindness, also known as protan defect, is related to red-green color blindness and color blindness. An important gene associated with Red Color Blindness is ISX (intestine-specific homeobox). Affiliated tissues include testes, and related mouse phenotype no phenotypic analysis.

Aliases & Classifications for Red Color Blindness

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8Disease Ontology, 10DISEASES, 22GTR, 60UMLS, 27ICD9CM, 56SNOMED-CT, 34MeSH
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Aliases & Descriptions:

red color blindness 8 10
protan defect 8 22
color blindness, red 60
protanopia 8


External Ids:

Disease Ontology8 DOID:13910
ICD9CM27 368.51
SNOMED-CT56 51445007
MeSH34 D003117

Related Diseases for Red Color Blindness

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17GeneCards, 18GeneDecks
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Diseases related to Red Color Blindness via text searches within MalaCards or GeneCards/GeneDecks gene sharing:

idRelated DiseaseScoreTop Affiliating Genes
1red-green color blindness10.4
2color blindness10.1
3red-green color vision defects10.1
4ocular albinism10.0
5albinism10.0
6colorblindness, protan10.0
7colorblindness, deutan10.0

Graphical network of diseases related to Red Color Blindness:



Diseases related to red color blindness

Clinical Features for Red Color Blindness

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Drugs & Therapeutics for Red Color Blindness

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Sources:
5CenterWatch, 41NIH Clinical Center, 6ClinicalTrials
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Approved drugs:

Search CenterWatch for Red Color Blindness

Drug clinical trials:

Search ClinicalTrials for Red Color Blindness

Search NIH Clinical Center for Red Color Blindness

Search CenterWatch for Red Color Blindness

Genetic Tests for Red Color Blindness

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22GTR
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Genetic tests related to Red Color Blindness:

id Genetic test Affiliating Genes
1 Protan Defect22

Anatomical Context for Red Color Blindness

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32MalaCards
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MalaCards organs/tissues related to Red Color Blindness:

32
Testes

Animal Models for Red Color Blindness or affiliated genes

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36MGI
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MGI Mouse Phenotypes related to Red Color Blindness:

36
idDescriptionMGI Source AccessionScoreTop Affiliating Genes
1MP:00030129.1RORC, ISX

Publications for Red Color Blindness

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50PubMed
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Articles related to Red Color Blindness:

idTitleAuthorsYear
1
Statistical and molecular analyses of evolutionary significance of red-green color vision and color blindness in vertebrates. (15647522)
2005
2
Red laser pointers and color blindness. (10076196)
1999
3
Bicuculline produces reversible red-green color blindness in goldfish, as revealed by monocular behavioral testing. (1663295)
1991
4
Incidence of red-green color blindness in the Basque population. (2378506)
1990
5
Spectral characteristics of electroretinography in congenital red-green color blindness. (3498068)
1987
6
Spectral characteristics of early receptor potential in congenital red-green color blindness. (3488889)
1986
7
Red color blindness. (100181)
1978
8
Criterion validity of four tests for red-green color blindness. (4536748)
1972
9
Red/green color blindness in the Niger delta. (5298588)
1967
10
Sex-linked nystagmus associated with red-green color-blindness. (17948382)
1949

Genetic Variations for Red Color Blindness

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Expression for genes affiliated with Red Color Blindness

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Sources:
1BioGPS, 15Gene Expression Omnibus DataSets
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Expression patterns in normal tissues for genes affiliated with Red Color Blindness

Search GEO for disease gene expression data for Red Color Blindness.

Pathways for genes affiliated with Red Color Blindness

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Compounds for genes affiliated with Red Color Blindness

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GO Terms for genes affiliated with Red Color Blindness

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Sources:
16Gene Ontology
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Molecular functions related to Red Color Blindness according to GeneCards/GeneDecks:

idNameGO IDScoreTop Affiliating Genes
1sequence-specific DNA bindingGO:0435659.1RORC, ISX

Products for genes affiliated with Red Color Blindness

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  • Antibodies
  • Proteins
  • Lysates
  • Antibodies

Sources for Red Color Blindness

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3CDC
13ExPASy
14FMA
22GTR
23HGMD
24HMDB
25ICD10
26ICD10 via Orphanet
27ICD9CM
28IUPHAR
29KEGG
34MeSH
35MESH via Orphanet
36MGI
39NCIt
40NDF-RT
43NINDS
44Novoseek
46OMIM
47OMIM via Orphanet
50PubMed
51QIAGEN
57SNOMED-CT via Orphanet
60UMLS
61UMLS via Orphanet