MCID: PRL014
MIFTS: 25

Paralytic Squint malady

Categories: Eye diseases, Neuronal diseases

Aliases & Classifications for Paralytic Squint

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Aliases & Descriptions for Paralytic Squint:

Name: Paralytic Squint 11 13
Paralytic Strabismus 11 66
 
Incomitant Dissociation 11

Classifications:



External Ids:

Disease Ontology11 DOID:10863
ICD1028 H49, H49.9
ICD9CM30 378.5, 378.50

Summaries for Paralytic Squint

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Wikipedia:69 Strabismus is a condition in which the eyes do not properly align with each other. This interferes with... more...

MalaCards based summary: Paralytic Squint, also known as paralytic strabismus, is related to abducens nerve disease and meckel syndrome 3, and has symptoms including ophthalmoplegia An important gene associated with Paralytic Squint is PHOX2A (Paired Like Homeobox 2a), and among its related pathways are Glypican 1 network and Signaling events mediated by PTP1B. Affiliated tissues include eye.

Related Diseases for Paralytic Squint

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Diseases related to Paralytic Squint via text searches within MalaCards or GeneCards Suite gene sharing:

(show top 50)    (show all 54)
idRelated DiseaseScoreTop Affiliating Genes
1abducens nerve disease23.8CADM1, CHN1, FUT2, GABBR1, HCK, KANTR
2meckel syndrome 310.6CHN1, KIF21A
3disuse amblyopia10.5CHN1, PHOX2A
4prolymphocytic leukemia10.5CADM1, CHN1
5endometriosis of rectovaginal septum and vagina10.4CHN1, KIF21A, PHOX2A
6mucopolysaccharidosis10.4CHN1, KIF21A, PHOX2A
7b-cell childhood acute lymphoblastic leukemia10.4CHN1, KIF21A, PHOX2A
8vaginal adenoma10.4CHN1, KIF21A, PHOX2A
9chandler syndrome10.4CHN1, KANTR
10adenosquamous breast carcinoma10.4CHN1, KANTR
11focal hand dystonia10.4FUT2, KANTR
12facial hemiatrophy10.3HCK, SAMHD1
13infant gynecomastia10.3HCK, KANTR
14myxoid chondrosarcoma10.3FUT2, KANTR
15deep corneal vascularisation10.3HCK, KANTR
16strabismus10.3
17autonomic neuropathy10.3HCK, SAMHD1
18kearns-sayre syndrome10.3
19chronic progressive external ophthalmoplegia10.3
20idiopathic juvenile osteoporosis10.3CHN1, KIF21A
21melanocytic psammomatous mpnst10.3KANTR, SAMHD1
22chronic inflammatory demyelinating polyneuritis10.3HCK, SAMHD1
23color agnosia10.3KANTR, PRNP
24brawny scleritis10.2FUT2, SAMHD1
25carotenemia10.2HCK, KANTR
26congenital fibrosis of the extraocular muscles10.2
27tolosa-hunt syndrome10.2
28neurilemmoma of the fifth cranial nerve10.1KANTR, SAMHD1
29gaze palsy, horizontal, with progressive scoliosis10.1
30progressive external ophthalmoplegia, autosomal recessive 110.1
31fourth cranial nerve palsy, familial congenital10.1
32total third-nerve palsy10.1
33fourth cranial nerve palsy10.1
34oculomotor nerve paralysis10.1
35trochlear nerve disease10.1
36autosomal dominant progressive external ophthalmoplegia10.1
37congenital trochlear nerve palsy10.1
38monofixation syndrome10.1CHN1, KIF21A, PHOX2A, SAMHD1
39long bones of lower limb cancer10.0CADM1, GABBR1, MTRNR2L5
40hypotropia10.0CHN1, KANTR, SAMHD1
41apraxia10.0KANTR, SAMHD1
42acrofrontofacionasal dysostosis10.0KANTR, PRNP
43lymphoepithelioma-like carcinoma9.9CHN1, KANTR, KIF21A, PHOX2A
44keratopathy9.9
45lyme disease9.9
46blepharospasm9.9
47tinea cruris9.8KANTR, SAMHD1
48meningocele9.8CHN1, HCK, PRL, PRNP
49interstitial emphysema9.8KANTR, SH3BP5
50accommodative esotropia9.8CHN1, KANTR, KIF21A, SAMHD1

Graphical network of the top 20 diseases related to Paralytic Squint:



Diseases related to paralytic squint

Symptoms for Paralytic Squint

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UMLS symptoms related to Paralytic Squint:


ophthalmoplegia

Drugs & Therapeutics for Paralytic Squint

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Interventional clinical trials:

Search ClinicalTrials, NIH Clinical Center for Paralytic Squint

Genetic Tests for Paralytic Squint

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Anatomical Context for Paralytic Squint

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MalaCards organs/tissues related to Paralytic Squint:

34
Eye

Animal Models for Paralytic Squint or affiliated genes

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Publications for Paralytic Squint

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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

Variations for Paralytic Squint

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Expression for genes affiliated with Paralytic Squint

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Search GEO for disease gene expression data for Paralytic Squint.

Pathways for genes affiliated with Paralytic Squint

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Pathways related to Paralytic Squint according to GeneCards Suite gene sharing:

idSuper pathwaysScoreTop Affiliating Genes
19.8HCK, PRNP
29.7HCK, PRL

GO Terms for genes affiliated with Paralytic Squint

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Sources for Paralytic Squint

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2CDC
6CNVD
10DGIdb
15ExPASy
16FDA
17FMA
25GTR
26HGMD
27HMDB
28ICD10
29ICD10 via Orphanet
30ICD9CM
31IUPHAR
32KEGG
35MedGen
37MeSH
38MESH via Orphanet
39MGI
42NCI
43NCIt
44NDF-RT
47NINDS
48Novoseek
50OMIM
51OMIM via Orphanet
55PubMed
56QIAGEN
61SNOMED-CT via Orphanet
65Tumor Gene Family of Databases
66UMLS
67UMLS via Orphanet