MCID: PRL014
MIFTS: 24

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 congenital fibrosis of the extraocular muscles and abducens nerve disease. 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 and liver.

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 46)
idRelated DiseaseScoreTop Affiliating Genes
1congenital fibrosis of the extraocular muscles10.6
2abducens nerve disease10.6
3chronic progressive external ophthalmoplegia10.6
4tolosa-hunt syndrome10.6
5kearns-sayre syndrome10.6
6gaze palsy, horizontal, with progressive scoliosis10.5
7progressive external ophthalmoplegia, autosomal recessive 110.5
8total third-nerve palsy10.5
9fourth cranial nerve palsy10.5
10oculomotor nerve paralysis10.5
11trochlear nerve disease10.5
12ophthalmoplegia10.5
13familial congenital fourth cranial nerve palsy10.5
14autosomal dominant progressive external ophthalmoplegia10.5
15maternally-inherited progressive external ophthalmoplegia10.5
16congenital trochlear nerve palsy10.5
17autism susceptibility 1710.3KIF21A, PHOX2A
18systemic lupus erythematosus10.3
19hiv-110.3
20alcoholic hepatitis10.3
21hepatitis10.3
22hypoplastic left heart syndrome10.3
23status epilepticus10.3
24vaginitis10.3
25long qt syndrome10.3
26neuronitis10.3
27lupus erythematosus10.3
28hemangioendothelioma10.3
29epithelioid hemangioendothelioma10.3
30meckel syndrome 310.3CHN1, KIF21A
31cyclotropia10.2CHN1, KIF21A
32amyotrophic neuralgia10.2CADM1, CHN1
33gallbladder disease10.2KIF21A, PHOX2A
34endometriosis in scar of skin10.1CHN1, KIF21A, PHOX2A
35hallucinogen abuse10.1CHN1, KIF21A, PHOX2A
36sensorineural hearing loss10.1KIF21A, PHOX2A, TUBB3
37breast-ovarian cancer, familial, 210.0CHN1, TUBB3
38clear cell adenoma10.0KIF21A, PHOX2A
39total circumpapillary dystrophy of choroid9.9CHN1, KIF21A, PHOX2A, TUBB3
40ametropic amblyopia9.9CHN1, KIF21A, PHOX2A, TUBB3
41kuhnt-junius degeneration9.9CHN1, PRL, PRNP
42water-clear cell adenoma9.9CHN1, KIF21A, PHOX2A, TUBB3
43thymus lymphoma9.9CADM1, MTRNR2L5
44nodular episcleritis9.7MTRNR2L5, PRL
45lipid-rich carcinoma9.6CHN1, KIF21A, MTRNR2L5, PHOX2A
46partial third-nerve palsy7.6CADM1, 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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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

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
Predictors of long term outcome of thoracic sympathectomy in complex regional pain syndrome (CRPS) type 2. (27155377)
2016
2
Transient lymphopenia breaks costimulatory blockade-based peripheral tolerance and initiates cardiac allograft rejection. (23834725)
2013
3
Early infantile cardiomyopathy and liver disease: a multisystemic disorder caused by congenital lipodystrophy. (23647707)
2013
4
Typical radiological findings of lipoid proteinosis of urbach and wiethe. A case report. (24207151)
2009
5
Factor XIIIA-V34L and factor XIIIB-H95R gene variants: effects on survival in myocardial infarction patients. (17515963)
2007
6
Effects of prednisolone treatment on cytokine expression in patients with leprosy type 1 reactions. (15908402)
2005
7
A new mutation in the myophosphorylase gene (Asn684Tyr) in a Spanish patient with McArdle's disease. (10382911)
1999
8
Epiglottitis in an immunized child. (3487780)
1986
9
Chondroblastoma of a metacarpal. Report of a case and review of the literature. (3884206)
1985

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