MCID: PRL014
MIFTS: 23

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 68
 
Incomitant Dissociation 11

Classifications:



External Ids:

Disease Ontology11 DOID:10863
ICD1030 H49, H49.9
ICD9CM32 378.5, 378.50

Summaries for Paralytic Squint

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Wikipedia:71 Strabismus, also called crossed eyes, is a condition in which the eyes do not properly align with each... 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 CHN1 (Chimerin 1), and among its related pathways is Glypican 1 network. 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 53)
idRelated DiseaseScoreTop Affiliating Genes
1abducens nerve disease24.4CADM1, CHN1, FUT2, GABBR1, HCK, KANTR
2meckel syndrome 310.5CHN1, 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
9adenosquamous breast carcinoma10.3CHN1, KANTR
10idiopathic juvenile osteoporosis10.3CHN1, KIF21A
11focal hand dystonia10.3FUT2, KANTR
12interstitial emphysema10.3KANTR, SH3BP5
13myxoid chondrosarcoma10.3FUT2, KANTR
14infant gynecomastia10.2HCK, KANTR
15deep corneal vascularisation10.2HCK, KANTR
16strabismus10.2
17autonomic neuropathy10.2HCK, SAMHD1
18kearns-sayre syndrome10.2
19melanocytic psammomatous mpnst10.2KANTR, SAMHD1
20color agnosia10.2KANTR, PRNP
21brawny scleritis10.2FUT2, SAMHD1
22chronic inflammatory demyelinating polyneuritis10.1HCK, SAMHD1
23carotenemia10.1HCK, KANTR
24tukel syndrome10.1
25chronic progressive external ophthalmoplegia10.1
26tolosa-hunt syndrome10.1
27monofixation syndrome10.0CHN1, KIF21A, PHOX2A, SAMHD1
28hypotropia10.0CHN1, KANTR, SAMHD1
29neurilemmoma of the fifth cranial nerve10.0KANTR, SAMHD1
30lymphoepithelioma-like carcinoma10.0CHN1, KANTR, KIF21A, PHOX2A
31gaze palsy, horizontal, with progressive scoliosis9.9
32progressive external ophthalmoplegia, autosomal recessive 19.9
33fourth cranial nerve palsy, familial congenital9.9
34total third-nerve palsy9.9
35fourth cranial nerve palsy9.9
36oculomotor nerve paralysis9.9
37trochlear nerve disease9.9
38autosomal dominant progressive external ophthalmoplegia9.9
39maternally-inherited progressive external ophthalmoplegia9.9
40congenital trochlear nerve palsy9.9
41apraxia9.9KANTR, SAMHD1
42acrofrontofacionasal dysostosis9.9KANTR, PRNP
43long bones of lower limb cancer9.8CADM1, GABBR1, MTRNR2L5
44tracheal stenosis9.8SAMHD1, SH3BP5
45accommodative esotropia9.8CHN1, KANTR, KIF21A, SAMHD1
46tinea cruris9.8KANTR, SAMHD1
47keratopathy9.8
48lyme disease9.8
49blepharospasm9.8
50meningocele9.7CHN1, HCK, PRL, PRNP

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



Diseases related to paralytic squint

Symptoms & Phenotypes 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:

36
Eye

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
19.7HCK, PRNP

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
27GTR
28HGMD
29HMDB
30ICD10
31ICD10 via Orphanet
32ICD9CM
33IUPHAR
34KEGG
37MedGen
39MeSH
40MESH via Orphanet
41MGI
44NCI
45NCIt
46NDF-RT
49NINDS
50Novoseek
52OMIM
53OMIM via Orphanet
57PubMed
58QIAGEN
63SNOMED-CT via Orphanet
67Tumor Gene Family of Databases
68UMLS
69UMLS via Orphanet