MCID: ACQ001
MIFTS: 25

Acquired Color Blindness

Categories: Eye diseases

Aliases & Classifications for Acquired Color Blindness

MalaCards integrated aliases for Acquired Color Blindness:

Name: Acquired Color Blindness 12 15
Acquired Color Vision Deficiencies 12
Acquired Color Vision Deficiency 12

Classifications:



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Disease Ontology 12 DOID:13912
ICD9CM 34 368.55
MeSH 43 D003117
NCIt 49 C118712
SNOMED-CT 67 71676008
ICD10 32 H53.52
UMLS 71 C0155018

Summaries for Acquired Color Blindness

MalaCards based summary : Acquired Color Blindness, also known as acquired color vision deficiencies, is related to intraocular pressure quantitative trait locus and rubeosis iridis. An important gene associated with Acquired Color Blindness is LAMA3 (Laminin Subunit Alpha 3). Affiliated tissues include eye, testes and prostate, and related phenotypes are Decreased viability with carboplatin and Decreased viability with carboplatin

Related Diseases for Acquired Color Blindness

Diseases in the Color Blindness family:

Acquired Color Blindness

Diseases related to Acquired Color Blindness via text searches within MalaCards or GeneCards Suite gene sharing:

(show all 46)
# Related Disease Score Top Affiliating Genes
1 intraocular pressure quantitative trait locus 28.8 PITX2 PAX6 FOXC1 EDNRA AQP4
2 rubeosis iridis 10.4 PRSS21 LAMA3
3 acute closed-angle glaucoma 10.4 LAMA3 DR1
4 axenfeld-rieger syndrome, type 2 10.3 PITX2 FOXC1
5 isolated aniridia 10.2 PAX6 FOXC1
6 cellular myxoid liposarcoma 10.2 CTAG1B CTAG1A
7 anterior segment dysgenesis 4 10.2 PITX2 FOXC1
8 epithelioid cell synovial sarcoma 10.2 CTAG1B CTAG1A
9 microvascular complications of diabetes 5 10.1
10 megalocornea 10.1 PITX2 FOXC1
11 congenital hypopituitarism 10.1 PITX2 PAX6
12 yemenite deaf-blind hypopigmentation syndrome 10.1
13 color blindness 10.1
14 color vision deficiency 10.1
15 hydrophthalmos 10.0 PITX2 PAX6 FOXC1
16 axenfeld-rieger syndrome, type 1 10.0 PITX2 PAX6 FOXC1
17 axenfeld-rieger syndrome 10.0 PITX2 PAX6 FOXC1
18 sclerocornea 10.0 PITX2 PAX6 FOXC1
19 juvenile glaucoma 10.0 PITX2 PAX6 FOXC1
20 axenfeld-rieger syndrome, type 3 10.0 PITX2 PAX6 FOXC1
21 intestinal atresia 10.0 PITX2 PAX6 FOXC1
22 iris disease 10.0 PITX2 PAX6 FOXC1
23 malignant renovascular hypertension 10.0 EDNRA CD2AP
24 persistent hyperplastic primary vitreous 10.0 PITX2 PAX6 FOXC1
25 primary congenital glaucoma 10.0 PITX2 PAX6 FOXC1
26 malignant hypertensive renal disease 10.0 EDNRA CD2AP
27 anterior segment dysgenesis 10.0 PITX2 PAX6 FOXC1
28 wilms tumor, aniridia, genitourinary anomalies, and mental retardation syndrome 10.0 PITX2 PAX6 FOXC1
29 cornea plana 10.0 PITX2 FOXC1
30 tritanopia 10.0
31 macular degeneration, age-related, 1 10.0
32 microvascular complications of diabetes 1 10.0
33 microvascular complications of diabetes 2 10.0
34 retinal vein occlusion 10.0
35 glaucoma 3, primary congenital, a 10.0 PITX2 PAX6 FOXC1
36 renal pelvis squamous cell carcinoma 10.0 F3 CD2AP
37 papillary adenofibroma 10.0 F3 CD2AP
38 aniridia 1 9.9 PITX2 PAX6 FOXC1
39 volkmann contracture 9.9 F3 CD2AP
40 vesiculobullous skin disease 9.9 LAMA3 DR1
41 atrial heart septal defect 9.9 PITX2 FOXC1 F3
42 coloboma of macula 9.8 PITX2 PAX6 FOXC1
43 syringomyelia 9.8 CD2AP AQP4
44 intracranial hypertension, idiopathic 9.8 F3 AQP4
45 intracranial hypertension 9.7 F3 ASRGL1 AQP4
46 peters-plus syndrome 9.7 PITX2 PAX6 FOXC1

Graphical network of the top 20 diseases related to Acquired Color Blindness:



Diseases related to Acquired Color Blindness

Symptoms & Phenotypes for Acquired Color Blindness

GenomeRNAi Phenotypes related to Acquired Color Blindness according to GeneCards Suite gene sharing:

26
# Description GenomeRNAi Source Accession Score Top Affiliating Genes
1 Decreased viability with carboplatin GR00207-A-7 9.23 EDNRA FOXC1
2 Decreased viability with carboplatin GR00207-A-9 9.23 EDNRA FOXC1

MGI Mouse Phenotypes related to Acquired Color Blindness:

45
# Description MGI Source Accession Score Top Affiliating Genes
1 respiratory system MP:0005388 9.5 AQP4 EDNRA F3 FOXC1 LAMA3 PAX6
2 vision/eye MP:0005391 9.17 AQP4 EDNRA F3 FOXC1 PAX6 PITX2

Drugs & Therapeutics for Acquired Color Blindness

Search Clinical Trials , NIH Clinical Center for Acquired Color Blindness

Genetic Tests for Acquired Color Blindness

Anatomical Context for Acquired Color Blindness

MalaCards organs/tissues related to Acquired Color Blindness:

40
Eye, Testes, Prostate, Heart, Skin

Publications for Acquired Color Blindness

Articles related to Acquired Color Blindness:

(show all 15)
# Title Authors PMID Year
1
Incidence of dyschromatopsy in glaucoma. 61
31705359 2019
2
Acquired color vision deficiency. 61
26656928 2016
3
Evaluation of Contrast Sensitivity, Chromatic Vision, and Reading Ability in Patients with Primary Open Angle Glaucoma. 61
27872754 2016
4
Ability of Bottle Cap Color to Facilitate Accurate Patient-Physician Communication Regarding Medication Identity in Patients with Glaucoma. 61
26260280 2015
5
Color vision deficiency in a middle-aged population: the Shahroud Eye Study. 61
24526316 2014
6
Evaluation of acquired color vision deficiency in glaucoma using the Rabin cone contrast test. 61
25168899 2014
7
A new color vision test to differentiate congenital and acquired color vision defects. 61
17296231 2007
8
Acquired color blindness in an elderly male patient from recurrent metastatic prostate cancer. 61
16108957 2005
9
Aviation-relevent epidemiology of color vision deficiency. 61
15742829 2005
10
Topography of the chromatic pattern-onset VEP. 61
12678619 2003
11
[Examination of confusion loci in acquired color vision deficiency with surface color]. 61
8317361 1993
12
Urinary glucose testing inaccuracies among diabetic patients. Effect of acquired color vision deficiency caused by diabetic retinopathy. 61
6333231 1984
13
Neuropathies of the optic nerve and visual evoked potentials with special reference to color vision and differential light threshold measured with the computer perimeter OCTOPUS. 61
6510191 1984
14
[Clinical value of the differential diagnosis between congenital and acquired color blindness]. 61
6969128 1980
15
[Boynton's method in acquired color blindness. II- Study of the neutral zones]. 61
6967778 1980

Variations for Acquired Color Blindness

Expression for Acquired Color Blindness

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

Pathways for Acquired Color Blindness

GO Terms for Acquired Color Blindness

Biological processes related to Acquired Color Blindness according to GeneCards Suite gene sharing:

# Name GO ID Score Top Affiliating Genes
1 positive regulation of transcription by RNA polymerase II GO:0045944 9.88 PITX2 PAX6 FOXC1 DR1 CTAG1B CTAG1A
2 camera-type eye development GO:0043010 9.5 PITX2 PAX6 FOXC1
3 iris morphogenesis GO:0061072 9.37 PITX2 PAX6
4 positive regulation of core promoter binding GO:1904798 9.26 PAX6 FOXC1
5 lacrimal gland development GO:0032808 9.16 PAX6 FOXC1
6 tRNA threonylcarbamoyladenosine metabolic process GO:0070525 8.96 CTAG1B CTAG1A
7 neural crest cell development GO:0014032 8.8 PDCD6 FOXC1 EDNRA

Molecular functions related to Acquired Color Blindness according to GeneCards Suite gene sharing:

# Name GO ID Score Top Affiliating Genes
1 transcription factor binding GO:0008134 8.92 PITX2 PAX6 FOXC1 DR1

Sources for Acquired Color Blindness

3 CDC
7 CNVD
9 Cosmic
10 dbSNP
11 DGIdb
17 EFO
18 ExPASy
19 FMA
28 GO
29 GTR
30 HMDB
31 HPO
32 ICD10
33 ICD10 via Orphanet
34 ICD9CM
35 IUPHAR
36 KEGG
37 LifeMap
39 LOVD
41 MedGen
43 MeSH
44 MESH via Orphanet
45 MGI
48 NCI
49 NCIt
50 NDF-RT
53 NINDS
54 Novoseek
56 OMIM
57 OMIM via Orphanet
61 PubMed
63 QIAGEN
68 SNOMED-CT via HPO
69 TGDB
70 Tocris
71 UMLS
72 UMLS via Orphanet
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