MCID: STH004

Saethre-Chotzen Syndrome, Fgfr2-Related malady

Categories: Genetic diseases, Rare diseases, Bone diseases, Eye diseases

Aliases & Classifications for Saethre-Chotzen Syndrome, Fgfr2-Related

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Aliases & Descriptions for Saethre-Chotzen Syndrome, Fgfr2-Related:

Name: Saethre-Chotzen Syndrome, Fgfr2-Related 24

Classifications:



Summaries for Saethre-Chotzen Syndrome, Fgfr2-Related

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MalaCards based summary: Saethre-Chotzen Syndrome, Fgfr2-Related An important gene associated with Saethre-Chotzen Syndrome, Fgfr2-Related is FGFR2 (Fibroblast Growth Factor Receptor 2).

Related Diseases for Saethre-Chotzen Syndrome, Fgfr2-Related

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Diseases in the Saethre-Chotzen Syndrome family:

saethre-chotzen syndrome, fgfr2-related

Symptoms & Phenotypes for Saethre-Chotzen Syndrome, Fgfr2-Related

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Drugs & Therapeutics for Saethre-Chotzen Syndrome, Fgfr2-Related

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Interventional clinical trials:

Search ClinicalTrials, NIH Clinical Center for Saethre-Chotzen Syndrome, Fgfr2-Related

Genetic Tests for Saethre-Chotzen Syndrome, Fgfr2-Related

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Genetic tests related to Saethre-Chotzen Syndrome, Fgfr2-Related:

id Genetic test Affiliating Genes
1 Saethre-Chotzen Syndrome, Fgfr2-Related24 FGFR2

Anatomical Context for Saethre-Chotzen Syndrome, Fgfr2-Related

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Publications for Saethre-Chotzen Syndrome, Fgfr2-Related

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Variations for Saethre-Chotzen Syndrome, Fgfr2-Related

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Expression for genes affiliated with Saethre-Chotzen Syndrome, Fgfr2-Related

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Search GEO for disease gene expression data for Saethre-Chotzen Syndrome, Fgfr2-Related.

Pathways for genes affiliated with Saethre-Chotzen Syndrome, Fgfr2-Related

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GO Terms for genes affiliated with Saethre-Chotzen Syndrome, Fgfr2-Related

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Sources for Saethre-Chotzen Syndrome, Fgfr2-Related

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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