MCID: PRL014
MIFTS: 23

Paralytic Squint malady

Eye, Neuronal categories

Summaries for Paralytic Squint

Sources:
64Wikipedia, 33MalaCards
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Wikipedia:64 Strabismus (/strəˈbɪzməs/, from Greek strabismós), also known as heterotropia (and including the... more...

MalaCards: Paralytic Squint, also known as paralytic strabismus, is related to strabismus and abducens palsy. An important gene associated with Paralytic Squint is PHOX2A (paired-like homeobox 2a). The compounds dopamine and norepinephrine have been mentioned in the context of this disorder.

Aliases & Classifications for Paralytic Squint

Sources:
8Disease Ontology, 10DISEASES, 61UMLS, 27ICD9CM, 57SNOMED-CT, 25ICD10
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Classifications:

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


Aliases & Descriptions:

paralytic squint 8 10
paralytic strabismus 8 61
paralytic strabismus, unspecified 8
unspecified paralytic strabismus 8
incomitant dissociation 8
paralytic squint nos 8


External Ids:

Disease Ontology8 DOID:10863
ICD9CM27 378.50, 378.5

Related Diseases for Paralytic Squint

Sources:
17GeneCards, 18GeneDecks
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Diseases related to Paralytic Squint via text searches within MalaCards or GeneCards/GeneDecks gene sharing:

idRelated DiseaseScoreTop Affiliating Genes
1strabismus10.5
2abducens palsy10.1
3blepharospasm10.1
4lyme disease10.1
5essential strabismus10.1

Graphical network of diseases related to Paralytic Squint:



Diseases related to paralytic squint

Clinical Features for Paralytic Squint

Drugs & Therapeutics for Paralytic Squint

Sources:
5CenterWatch, 42NIH Clinical Center, 6ClinicalTrials
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Approved drugs:

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Drug clinical trials:

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Search NIH Clinical Center for Paralytic Squint

Search CenterWatch for Paralytic Squint

Genetic Tests for Paralytic Squint

Anatomical Context for Paralytic Squint

Animal Models for Paralytic Squint or affiliated genes

Sources:
28inGenious Targeting Laboratory
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Publications for Paralytic Squint

Sources:
51PubMed
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Articles related to Paralytic Squint:

idTitleAuthorsYear
1
Paralytic squint due to abducens nerve palsy: a rare consequence of dengue fever. (22799448)
2012
2
Paralytic squint treated with acupuncture. (6570146)
1984
3
The use of prisms in paralytic squint. (900621)
1977
4
A surgery on twenty six thousand and three hundred seventy eight patients with convergent squint (26378), thirteen thousand, one hundred and eighty one patients with divergent squint (13181), one thousand and twenty nine patients of vertical squint (1029), ten thousand and one hundred thirty nine patients of heterophoria (10139) and two thousand sixty one patients of paralytic squint (2061) seen during the past ten years at Giza Ophthalmic Hospital Squint Clinic from the year 1960 to the year 1970. (4666806)
1972
5
Diagnosis of paralytic squint. (5154750)
1971
6
NON-PARALYTIC squint. (13450382)
1957
7
Paralytic squint. (20295367)
1947
8
Clinical orthoptic procedure: paralytic squint. (20295365)
1947
9
SOME CASES OF PARALYTIC SQUINT. (18169478)
1937

Genetic Variations for Paralytic Squint

Expression for genes affiliated with Paralytic Squint

Sources:
1BioGPS, 15Gene Expression Omnibus DataSets
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Expression patterns in normal tissues for genes affiliated with Paralytic Squint

Search GEO for disease gene expression data for Paralytic Squint.

Pathways for genes affiliated with Paralytic Squint

Compounds for genes affiliated with Paralytic Squint

Sources:
45Novoseek, 29IUPHAR, 11DrugBank, 24HMDB
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Compounds related to Paralytic Squint according to GeneCards/GeneDecks:

idCompoundScoreTop Affiliating Genes
1dopamine45 29 11 2412.4PHOX2A, GABBR1
2norepinephrine45 11 2411.1PHOX2A, GABBR1

GO Terms for genes affiliated with Paralytic Squint

Products for genes affiliated with Paralytic Squint

  • Antibodies
  • Proteins
  • Lysates
  • Antibodies

Sources for Paralytic Squint

3CDC
13ExPASy
14FMA
22GTR
23HGMD
24HMDB
25ICD10
26ICD10 via Orphanet
27ICD9CM
29IUPHAR
30KEGG
35MeSH
36MESH via Orphanet
37MGI
40NCIt
41NDF-RT
44NINDS
45Novoseek
47OMIM
48OMIM via Orphanet
51PubMed
52QIAGEN
58SNOMED-CT via Orphanet
61UMLS
62UMLS via Orphanet