MCID: SLX001

Slx4-Related Fanconi Anemia malady

Genetic diseases, Rare diseases, Blood diseases categories
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Summaries for Slx4-Related Fanconi Anemia

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MalaCards based summary: Slx4-Related Fanconi Anemia An important gene associated with Slx4-Related Fanconi Anemia is SLX4 (SLX4 structure-specific endonuclease subunit).

Aliases & Classifications for Slx4-Related Fanconi Anemia

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Slx4-Related Fanconi Anemia, Aliases & Descriptions:

Name: Slx4-Related Fanconi Anemia 20


Classifications:

Malacards categories (disease lists): (See all malacards categories)
Global: Genetic diseases, Rare diseases
Anatomical: Blood diseases


Related Diseases for Slx4-Related Fanconi Anemia

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Symptoms for Slx4-Related Fanconi Anemia

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Drugs & Therapeutics for Slx4-Related Fanconi Anemia

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Drug clinical trials:

Search ClinicalTrials for Slx4-Related Fanconi Anemia

Search NIH Clinical Center for Slx4-Related Fanconi Anemia

Genetic Tests for Slx4-Related Fanconi Anemia

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Genetic tests related to Slx4-Related Fanconi Anemia:

id Genetic test Affiliating Genes
1 Slx4-Related Fanconi Anemia20 SLX4

Anatomical Context for Slx4-Related Fanconi Anemia

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Animal Models for Slx4-Related Fanconi Anemia or affiliated genes

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Publications for Slx4-Related Fanconi Anemia

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Variations for Slx4-Related Fanconi Anemia

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Expression for genes affiliated with Slx4-Related Fanconi Anemia

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Expression patterns in normal tissues for genes affiliated with Slx4-Related Fanconi Anemia

Search GEO for disease gene expression data for Slx4-Related Fanconi Anemia.

Pathways for genes affiliated with Slx4-Related Fanconi Anemia

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Compounds for genes affiliated with Slx4-Related Fanconi Anemia

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GO Terms for genes affiliated with Slx4-Related Fanconi Anemia

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Products for genes affiliated with Slx4-Related Fanconi Anemia

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  • Antibodies
  • Proteins
  • Lysates

Sources for Slx4-Related Fanconi Anemia

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3CDC
13ExPASy
14FMA
22GTR
23HGMD
24HMDB
25ICD10
26ICD10 via Orphanet
27ICD9CM
28IUPHAR
29KEGG
34MeSH
35MESH via Orphanet
36MGI
39NCIt
40NDF-RT
43NINDS
44Novoseek
46OMIM
47OMIM via Orphanet
51PubMed
52QIAGEN
58SNOMED-CT via Orphanet
62UMLS
63UMLS via Orphanet