MCID: FGS005

Fg Syndrome Type 1 malady

Genetic diseases (common) category
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Summaries for Fg Syndrome Type 1

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33MalaCards
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MalaCards: Fg Syndrome Type 1, also known as fg syndrome, is related to focal segmental glomerulosclerosis. An important gene associated with Fg Syndrome Type 1 is MED12 (mediator complex subunit 12).

Aliases & Classifications for Fg Syndrome Type 1

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62UMLS, 20GeneTests
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Classifications:

Malacards categories (disease lists): (See all malacards categories)
Global: Genetic diseases (common)


Aliases & Descriptions:

fg syndrome type 1 20
fg syndrome 62


Related Diseases for Fg Syndrome Type 1

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17GeneCards, 18GeneDecks
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Diseases related to Fg Syndrome Type 1 via text searches within MalaCards or GeneCards/GeneDecks gene sharing:

idRelated DiseaseScoreTop Affiliating Genes
1focal segmental glomerulosclerosis10.2

Symptoms for Fg Syndrome Type 1

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Drugs & Therapeutics for Fg Syndrome Type 1

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Sources:
42NIH Clinical Center, 6ClinicalTrials
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Drug clinical trials:

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Search NIH Clinical Center for Fg Syndrome Type 1

Genetic Tests for Fg Syndrome Type 1

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Sources:
20GeneTests
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Genetic tests related to Fg Syndrome Type 1:

id Genetic test Affiliating Genes
1 Fg Syndrome Type 120 MED12

Anatomical Context for Fg Syndrome Type 1

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Animal Models for Fg Syndrome Type 1 or affiliated genes

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Publications for Fg Syndrome Type 1

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Variations for Fg Syndrome Type 1

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Expression for genes affiliated with Fg Syndrome Type 1

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Sources:
2BioGPS, 15Gene Expression Omnibus DataSets
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Expression patterns in normal tissues for genes affiliated with Fg Syndrome Type 1

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Pathways for genes affiliated with Fg Syndrome Type 1

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Compounds for genes affiliated with Fg Syndrome Type 1

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GO Terms for genes affiliated with Fg Syndrome Type 1

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Products for genes affiliated with Fg Syndrome Type 1

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  • Antibodies
  • Proteins
  • Lysates
  • Antibodies

Sources for Fg Syndrome Type 1

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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