MCID: RDC001
MIFTS: 17

Red Color Blindness malady

Eye diseases category

Summaries for Red Color Blindness

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MalaCards based summary: Red Color Blindness, also known as protan defect, is related to color blindness and blindness. An important gene associated with Red Color Blindness is OPN1LW (opsin 1 (cone pigments), long-wave-sensitive). Affiliated tissues include eye.

Aliases & Classifications for Red Color Blindness

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Red Color Blindness, Aliases & Descriptions:

Name: Red Color Blindness 9 11
Protan Defect 9 23
 
Color Blindness, Red 61
Protanopia 9


Classifications:

Malacards categories (disease lists): (See all malacards categories)
Anatomical: Eye diseases


External Ids:

Disease Ontology9 DOID:13910
MeSH34 D003117
SNOMED-CT56 51445007
ICD9CM28 368.51

Related Diseases for Red Color Blindness

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

idRelated DiseaseScoreTop Affiliating Genes
1color blindness10.2
2blindness10.2
3ocular albinism10.1
4albinism10.1
5colorblindness, protan10.1
6colorblindness, deutan10.1

Graphical network of diseases related to Red Color Blindness:



Diseases related to red color blindness

Symptoms for Red Color Blindness

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Drugs & Therapeutics for Red Color Blindness

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Drug clinical trials:

Search ClinicalTrials for Red Color Blindness

Search NIH Clinical Center for Red Color Blindness

Genetic Tests for Red Color Blindness

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Genetic tests related to Red Color Blindness:

id Genetic test Affiliating Genes
1 Protan Defect23

Anatomical Context for Red Color Blindness

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MalaCards organs/tissues related to Red Color Blindness:

32
Eye

Animal Models for Red Color Blindness or affiliated genes

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Publications for Red Color Blindness

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Articles related to Red Color Blindness:

idTitleAuthorsYear
1
Red color blindness. (100181)
1978

Variations for Red Color Blindness

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Clinvar genetic disease variations for Red Color Blindness:

7
id Gene Name Type Significance SNP ID Assembly Location
1OPN1LWNM_020061.5(OPN1LW): c.1013G> A (p.Gly338Glu)single nucleotide variantPathogenicrs104894913GRCh37Chr X, 153424319: 153424319

Expression for genes affiliated with Red Color Blindness

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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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Products for genes affiliated with Red Color Blindness

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  • Antibodies
  • Proteins
  • Lysates
  • Antibodies
  • Proteins
  • Kits and Assays

Sources for Red Color Blindness

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4CDC
14ExPASy
15FMA
23GTR
24HGMD
25HMDB
26ICD10
27ICD10 via Orphanet
28ICD9CM
29IUPHAR
30KEGG
34MeSH
35MESH via Orphanet
36MGI
39NCIt
40NDF-RT
43NINDS
44Novoseek
46OMIM
47OMIM via Orphanet
51PubMed
52QIAGEN
57SNOMED-CT via Orphanet
61UMLS
62UMLS via Orphanet