MCID: FGS005

Fg Syndrome Type 1 malady

Genetic diseases (common) category

Summaries for Fg Syndrome Type 1

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MalaCards based summary: Fg Syndrome Type 1 is related to fg syndrome. 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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Fg Syndrome Type 1, Aliases & Descriptions:

Name: Fg Syndrome Type 1 21


Classifications:

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


Related Diseases for Fg Syndrome Type 1

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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
1fg syndrome10.3

Symptoms for Fg Syndrome Type 1

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Drugs & Therapeutics for Fg Syndrome Type 1

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Drug clinical trials:

Search ClinicalTrials for Fg Syndrome Type 1

Search NIH Clinical Center for Fg Syndrome Type 1

Genetic Tests for Fg Syndrome Type 1

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Genetic tests related to Fg Syndrome Type 1:

id Genetic test Affiliating Genes
1 Fg Syndrome Type 121 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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Expression patterns in normal tissues for genes affiliated with Fg Syndrome Type 1

Search GEO for disease gene expression data for Fg Syndrome Type 1.

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
  • Proteins
  • Kits and Assays

Sources for Fg Syndrome Type 1

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4CDC
14ExPASy
15FMA
23GTR
24HGMD
25HMDB
26ICD10
27ICD10 via Orphanet
28ICD9CM
29IUPHAR
30KEGG
34MeSH
35MESH via Orphanet
36MGI
39NCIt
40NDF-RT
43NINDS
44Novoseek
46OMIM
47OMIM via Orphanet
51PubMed
52QIAGEN
57SNOMED-CT via Orphanet
61UMLS
62UMLS via Orphanet