MCID: BRR001
MIFTS: 12

Barre-Lieou Syndrome malady

Aliases & Classifications for Barre-Lieou Syndrome

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Aliases & Descriptions for Barre-Lieou Syndrome:

Name: Barre-Lieou Syndrome 10 12
Posterior Cervical Sympathetic Syndrome 10 36 65
 
Cervicocranial Syndrome 10 65

Classifications:



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Disease Ontology10 DOID:6692
ICD1027 M53.0
SNOMED-CT59 17300000
MeSH36 D055010
NCIt42 C34411
UMLS65 C0376378, C2355645

Summaries for Barre-Lieou Syndrome

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Disease Ontology:10 A syndrome that involves occipital head aches, nystagmus on head movement, tinnitus, spasms, blurred vision, corneal hyperaesthesia, and corneal ulcers.

MalaCards based summary: Barre-Lieou Syndrome, also known as posterior cervical sympathetic syndrome, is related to vaginal adenoma and testicular monophasic choriocarcinoma. An important gene associated with Barre-Lieou Syndrome is PPP1R3C (Protein Phosphatase 1 Regulatory Subunit 3C), and among its related pathways are Translation Insulin regulation of translation and p70S6K Signaling.

Related Diseases for Barre-Lieou Syndrome

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Diseases related to Barre-Lieou Syndrome via text searches within MalaCards or GeneCards Suite gene sharing:

idRelated DiseaseScoreTop Affiliating Genes
1vaginal adenoma9.7PPP1R3B, PPP1R3C
2testicular monophasic choriocarcinoma9.5PPP1R3B, PPP1R3C

Symptoms for Barre-Lieou Syndrome

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Drugs & Therapeutics for Barre-Lieou Syndrome

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Interventional clinical trials:

Search ClinicalTrials, NIH Clinical Center for Barre-Lieou Syndrome


Cochrane evidence based reviews: posterior cervical sympathetic syndrome

Genetic Tests for Barre-Lieou Syndrome

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Anatomical Context for Barre-Lieou Syndrome

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Animal Models for Barre-Lieou Syndrome or affiliated genes

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Publications for Barre-Lieou Syndrome

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Variations for Barre-Lieou Syndrome

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Expression for genes affiliated with Barre-Lieou Syndrome

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Search GEO for disease gene expression data for Barre-Lieou Syndrome.

Pathways for genes affiliated with Barre-Lieou Syndrome

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GO Terms for genes affiliated with Barre-Lieou Syndrome

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Sources for Barre-Lieou Syndrome

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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