MCID: FGR001

Fga-Related Congenital Afibrinogenemia malady

Genetic diseases, Rare diseases, Blood diseases categories

Aliases & Classifications for Fga-Related Congenital Afibrinogenemia

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Aliases & Descriptions for Fga-Related Congenital Afibrinogenemia:

Name: Fga-Related Congenital Afibrinogenemia 20


Classifications:



Summaries for Fga-Related Congenital Afibrinogenemia

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MalaCards based summary: Fga-Related Congenital Afibrinogenemia An important gene associated with Fga-Related Congenital Afibrinogenemia is FGA (fibrinogen alpha chain).

Related Diseases for Fga-Related Congenital Afibrinogenemia

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Symptoms for Fga-Related Congenital Afibrinogenemia

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Drugs & Therapeutics for Fga-Related Congenital Afibrinogenemia

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Drug clinical trials:

Search ClinicalTrials for Fga-Related Congenital Afibrinogenemia

Search NIH Clinical Center for Fga-Related Congenital Afibrinogenemia

Genetic Tests for Fga-Related Congenital Afibrinogenemia

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Genetic tests related to Fga-Related Congenital Afibrinogenemia:

id Genetic test Affiliating Genes
1 Fga-Related Congenital Afibrinogenemia20 FGA

Anatomical Context for Fga-Related Congenital Afibrinogenemia

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Animal Models for Fga-Related Congenital Afibrinogenemia or affiliated genes

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Publications for Fga-Related Congenital Afibrinogenemia

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Variations for Fga-Related Congenital Afibrinogenemia

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Expression for genes affiliated with Fga-Related Congenital Afibrinogenemia

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Search GEO for disease gene expression data for Fga-Related Congenital Afibrinogenemia.

Pathways for genes affiliated with Fga-Related Congenital Afibrinogenemia

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Compounds for genes affiliated with Fga-Related Congenital Afibrinogenemia

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GO Terms for genes affiliated with Fga-Related Congenital Afibrinogenemia

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Sources for Fga-Related Congenital Afibrinogenemia

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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