MCID: FGR002

Fga-Related Familial Visceral Amyloidosis malady

Categories: Genetic diseases, Rare diseases, Nephrological diseases, Bone diseases, Metabolic diseases, Neuronal diseases

Aliases & Classifications for Fga-Related Familial Visceral Amyloidosis

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Aliases & Descriptions for Fga-Related Familial Visceral Amyloidosis:

Name: Fga-Related Familial Visceral Amyloidosis 24

Classifications:



Summaries for Fga-Related Familial Visceral Amyloidosis

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MalaCards based summary: Fga-Related Familial Visceral Amyloidosis An important gene associated with Fga-Related Familial Visceral Amyloidosis is FGA (Fibrinogen Alpha Chain).

Related Diseases for Fga-Related Familial Visceral Amyloidosis

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Symptoms & Phenotypes for Fga-Related Familial Visceral Amyloidosis

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Drugs & Therapeutics for Fga-Related Familial Visceral Amyloidosis

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Interventional clinical trials:

Search ClinicalTrials, NIH Clinical Center for Fga-Related Familial Visceral Amyloidosis

Genetic Tests for Fga-Related Familial Visceral Amyloidosis

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Genetic tests related to Fga-Related Familial Visceral Amyloidosis:

id Genetic test Affiliating Genes
1 Fga-Related Familial Visceral Amyloidosis24 FGA

Anatomical Context for Fga-Related Familial Visceral Amyloidosis

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Publications for Fga-Related Familial Visceral Amyloidosis

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Variations for Fga-Related Familial Visceral Amyloidosis

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Expression for genes affiliated with Fga-Related Familial Visceral Amyloidosis

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Search GEO for disease gene expression data for Fga-Related Familial Visceral Amyloidosis.

Pathways for genes affiliated with Fga-Related Familial Visceral Amyloidosis

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GO Terms for genes affiliated with Fga-Related Familial Visceral Amyloidosis

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Sources for Fga-Related Familial Visceral Amyloidosis

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2CDC
6CNVD
10DGIdb
15ExPASy
16FDA
17FMA
27GTR
28HGMD
29HMDB
30ICD10
31ICD10 via Orphanet
32ICD9CM
33IUPHAR
34KEGG
37MedGen
39MeSH
40MESH via Orphanet
41MGI
44NCI
45NCIt
46NDF-RT
49NINDS
50Novoseek
52OMIM
53OMIM via Orphanet
57PubMed
58QIAGEN
63SNOMED-CT via Orphanet
67Tumor Gene Family of Databases
68UMLS
69UMLS via Orphanet