MCID: F5R001

F5-Related Budd-Chiari Syndrome malady

Genetic diseases, Rare diseases, Cardiovascular diseases, Gastrointestinal diseases, Liver diseases, Blood diseases, Mental diseases categories

Aliases & Classifications for F5-Related Budd-Chiari Syndrome

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Aliases & Descriptions for F5-Related Budd-Chiari Syndrome:

Name: F5-Related Budd-Chiari Syndrome 20


Classifications:



Summaries for F5-Related Budd-Chiari Syndrome

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MalaCards based summary: F5-Related Budd-Chiari Syndrome An important gene associated with F5-Related Budd-Chiari Syndrome is F5 (coagulation factor V (proaccelerin, labile factor)).

Related Diseases for F5-Related Budd-Chiari Syndrome

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Diseases in the Budd-Chiari Syndrome family:

f5-related budd-chiari syndrome Jak2-Related Budd-Chiari Syndrome

Symptoms for F5-Related Budd-Chiari Syndrome

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Drugs & Therapeutics for F5-Related Budd-Chiari Syndrome

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Drug clinical trials:

Search ClinicalTrials for F5-Related Budd-Chiari Syndrome

Search NIH Clinical Center for F5-Related Budd-Chiari Syndrome

Genetic Tests for F5-Related Budd-Chiari Syndrome

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Genetic tests related to F5-Related Budd-Chiari Syndrome:

id Genetic test Affiliating Genes
1 F5-Related Budd-Chiari Syndrome20 F5

Anatomical Context for F5-Related Budd-Chiari Syndrome

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Animal Models for F5-Related Budd-Chiari Syndrome or affiliated genes

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Publications for F5-Related Budd-Chiari Syndrome

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Variations for F5-Related Budd-Chiari Syndrome

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Expression for genes affiliated with F5-Related Budd-Chiari Syndrome

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Search GEO for disease gene expression data for F5-Related Budd-Chiari Syndrome.

Pathways for genes affiliated with F5-Related Budd-Chiari Syndrome

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Compounds for genes affiliated with F5-Related Budd-Chiari Syndrome

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GO Terms for genes affiliated with F5-Related Budd-Chiari Syndrome

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Sources for F5-Related Budd-Chiari Syndrome

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2CDC
12ExPASy
13FDA
14FMA
22GTR
23HGMD
24HMDB
25ICD10
26ICD10 via Orphanet
27ICD9CM
28IUPHAR
29KEGG
33MeSH
34MESH via Orphanet
35MGI
38NCI
39NCIt
40NDF-RT
43NINDS
44Novoseek
46OMIM
47OMIM via Orphanet
51PubMed
52QIAGEN
57SNOMED-CT via Orphanet
61UMLS
62UMLS via Orphanet