MCID: DYS080

Dysfibrinogenemia, Gamma Type malady

Genetic diseases, Rare diseases categories
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Summaries for Dysfibrinogenemia, Gamma Type

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33MalaCards
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MalaCards: Dysfibrinogenemia, Gamma Type An important gene associated with Dysfibrinogenemia, Gamma Type is FGG (fibrinogen gamma chain).

Aliases & Classifications for Dysfibrinogenemia, Gamma Type

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47OMIM
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Classifications:

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Global: Genetic diseases, Rare diseases


Aliases & Descriptions:

dysfibrinogenemia, gamma type 47


Related Diseases for Dysfibrinogenemia, Gamma Type

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Diseases in the Dysfibrinogenemia family:

Dysfibrinogenemia, Beta Type dysfibrinogenemia, gamma type

Symptoms for Dysfibrinogenemia, Gamma Type

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Drugs & Therapeutics for Dysfibrinogenemia, Gamma Type

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42NIH Clinical Center, 6ClinicalTrials
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Drug clinical trials:

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Genetic Tests for Dysfibrinogenemia, Gamma Type

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Anatomical Context for Dysfibrinogenemia, Gamma Type

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Animal Models for Dysfibrinogenemia, Gamma Type or affiliated genes

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Publications for Dysfibrinogenemia, Gamma Type

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Variations for Dysfibrinogenemia, Gamma Type

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Expression for genes affiliated with Dysfibrinogenemia, Gamma Type

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2BioGPS, 15Gene Expression Omnibus DataSets
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Expression patterns in normal tissues for genes affiliated with Dysfibrinogenemia, Gamma Type

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Pathways for genes affiliated with Dysfibrinogenemia, Gamma Type

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Compounds for genes affiliated with Dysfibrinogenemia, Gamma Type

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GO Terms for genes affiliated with Dysfibrinogenemia, Gamma Type

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Products for genes affiliated with Dysfibrinogenemia, Gamma Type

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  • Antibodies
  • Proteins
  • Lysates
  • Antibodies

Sources for Dysfibrinogenemia, Gamma Type

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4CDC
13ExPASy
14FMA
22GTR
23HGMD
24HMDB
25ICD10
26ICD10 via Orphanet
27ICD9CM
29IUPHAR
30KEGG
35MeSH
36MESH via Orphanet
37MGI
40NCIt
41NDF-RT
44NINDS
45Novoseek
47OMIM
48OMIM via Orphanet
52PubMed
53QIAGEN
59SNOMED-CT via Orphanet
62UMLS
63UMLS via Orphanet