MCID: PRL014
MIFTS: 27

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 10 12
Paralytic Strabismus 10 65
 
Incomitant Dissociation 10

Classifications:



External Ids:

Disease Ontology10 DOID:10863
ICD1027 H49, H49.9
ICD9CM29 378.5, 378.50
UMLS65 C0152221

Summaries for Paralytic Squint

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Wikipedia:68 Strabismus is a condition that interferes with binocular vision because it prevents a person from... more...

MalaCards based summary: Paralytic Squint, also known as paralytic strabismus, is related to autism susceptibility 17 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 is Prion diseases. Affiliated tissues include eye, liver and thymus.

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 all 38)
idRelated DiseaseScoreTop Affiliating Genes
1autism susceptibility 1710.5KIF21A, PHOX2A
2meckel syndrome 310.4CHN1, KIF21A
3strabismus10.3
4cyclotropia10.3CHN1, KIF21A
5amyotrophic neuralgia10.3CADM1, CHN1
6gallbladder disease10.3KIF21A, PHOX2A
7congenital fibrosis of the extraocular muscles10.2
8abducens nerve disease10.2
9chronic progressive external ophthalmoplegia10.2
10tolosa-hunt syndrome10.2
11kearns-sayre syndrome10.2
12endometriosis in scar of skin10.2CHN1, KIF21A, PHOX2A
13hallucinogen abuse10.2CHN1, KIF21A, PHOX2A
14sensorineural hearing loss10.1KIF21A, PHOX2A, TUBB3
15gaze palsy, horizontal, with progressive scoliosis10.1
16progressive external ophthalmoplegia, autosomal recessive 110.1
17total third-nerve palsy10.1
18fourth cranial nerve palsy10.1
19oculomotor nerve paralysis10.1
20trochlear nerve disease10.1
21ophthalmoplegia10.1
22familial congenital fourth cranial nerve palsy10.1
23autosomal dominant progressive external ophthalmoplegia10.1
24maternally-inherited progressive external ophthalmoplegia10.1
25congenital trochlear nerve palsy10.1
26breast-ovarian cancer, familial, 210.0CHN1, TUBB3
27clear cell adenoma10.0KIF21A, PHOX2A
28keratopathy9.9
29lyme disease9.9
30blepharospasm9.9
31total circumpapillary dystrophy of choroid9.9CHN1, KIF21A, PHOX2A, TUBB3
32ametropic amblyopia9.9CHN1, KIF21A, PHOX2A, TUBB3
33kuhnt-junius degeneration9.9CHN1, PRL, PRNP
34water-clear cell adenoma9.8CHN1, KIF21A, PHOX2A, TUBB3
35thymus lymphoma9.8CADM1, MTRNR2L5
36nodular episcleritis9.5MTRNR2L5, PRL
37lipid-rich carcinoma9.5CHN1, KIF21A, MTRNR2L5, PHOX2A
38partial third-nerve palsy6.4CADM1, CHN1, FUT2, KIF21A, MTRNR2L5, PHOX2A

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:

33
Eye, Liver, Thymus, Heart, Breast, Skin

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
19.7PHOX2A, PRNP

GO Terms for genes affiliated with Paralytic Squint

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Sources for Paralytic Squint

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2CDC
14ExPASy
15FDA
16FMA
24GTR
25HGMD
26HMDB
27ICD10
28ICD10 via Orphanet
29ICD9CM
30IUPHAR
31KEGG
34MedGen
36MeSH
37MESH via Orphanet
38MGI
41NCI
42NCIt
43NDF-RT
46NINDS
47Novoseek
49OMIM
50OMIM via Orphanet
54PubMed
55QIAGEN
60SNOMED-CT via Orphanet
64Tumor Gene Family of Databases
65UMLS
66UMLS via Orphanet