MCID: FGF005
MIFTS: 2

Fgfr2-Related Isolated Coronal Synostosis malady

Categories: Genetic diseases

Aliases & Classifications for Fgfr2-Related Isolated Coronal Synostosis

Aliases & Descriptions for Fgfr2-Related Isolated Coronal Synostosis:

Name: Fgfr2-Related Isolated Coronal Synostosis 24

Classifications:



Summaries for Fgfr2-Related Isolated Coronal Synostosis

MalaCards based summary : Fgfr2-Related Isolated Coronal Synostosis An important gene associated with Fgfr2-Related Isolated Coronal Synostosis is FGFR2 (Fibroblast Growth Factor Receptor 2).

Related Diseases for Fgfr2-Related Isolated Coronal Synostosis

Diseases in the Fgfr3-Related Isolated Coronal Synostosis family:

Fgfr2-Related Isolated Coronal Synostosis

Symptoms & Phenotypes for Fgfr2-Related Isolated Coronal Synostosis

Drugs & Therapeutics for Fgfr2-Related Isolated Coronal Synostosis

Search Clinical Trials , NIH Clinical Center for Fgfr2-Related Isolated Coronal Synostosis

Genetic Tests for Fgfr2-Related Isolated Coronal Synostosis

Genetic tests related to Fgfr2-Related Isolated Coronal Synostosis:

id Genetic test Affiliating Genes
1 Fgfr2-Related Isolated Coronal Synostosis 24 FGFR2

Anatomical Context for Fgfr2-Related Isolated Coronal Synostosis

Publications for Fgfr2-Related Isolated Coronal Synostosis

Variations for Fgfr2-Related Isolated Coronal Synostosis

Expression for Fgfr2-Related Isolated Coronal Synostosis

Search GEO for disease gene expression data for Fgfr2-Related Isolated Coronal Synostosis.

Pathways for Fgfr2-Related Isolated Coronal Synostosis

GO Terms for Fgfr2-Related Isolated Coronal Synostosis

Sources for Fgfr2-Related Isolated Coronal Synostosis

3 CDC
7 CNVD
9 Cosmic
10 dbSNP
11 DGIdb
16 ExPASy
18 FMA
28 GO
29 GTR
30 HGMD
31 HMDB
32 HPO
33 ICD10
34 ICD10 via Orphanet
35 ICD9CM
36 IUPHAR
37 KEGG
38 LifeMap
40 MedGen
42 MeSH
43 MESH via Orphanet
44 MGI
46 NCI
47 NCIt
48 NDF-RT
51 NINDS
52 Novoseek
54 OMIM
55 OMIM via Orphanet
59 PubMed
60 QIAGEN
65 SNOMED-CT via Orphanet
67 TGDB
68 Tocris
69 UMLS
70 UMLS via Orphanet
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