MCID: FGF003
MIFTS: 7

Fgfr1-Related Craniosynostosis malady

Categories: Genetic diseases, Bone diseases, Fetal diseases, Rare diseases

Aliases & Classifications for Fgfr1-Related Craniosynostosis

Aliases & Descriptions for Fgfr1-Related Craniosynostosis:

Name: Fgfr1-Related Craniosynostosis 24
Craniosynostosis Syndromes, Fgfr1-Related 24

Classifications:



Summaries for Fgfr1-Related Craniosynostosis

MalaCards based summary : Fgfr1-Related Craniosynostosis, is also known as craniosynostosis syndromes, fgfr1-related. An important gene associated with Fgfr1-Related Craniosynostosis is FGFR1 (Fibroblast Growth Factor Receptor 1).

Related Diseases for Fgfr1-Related Craniosynostosis

Symptoms & Phenotypes for Fgfr1-Related Craniosynostosis

Drugs & Therapeutics for Fgfr1-Related Craniosynostosis

Search Clinical Trials , NIH Clinical Center for Fgfr1-Related Craniosynostosis

Genetic Tests for Fgfr1-Related Craniosynostosis

Genetic tests related to Fgfr1-Related Craniosynostosis:

id Genetic test Affiliating Genes
1 Fgfr1-Related Craniosynostosis 24 FGFR1

Anatomical Context for Fgfr1-Related Craniosynostosis

Publications for Fgfr1-Related Craniosynostosis

Variations for Fgfr1-Related Craniosynostosis

Expression for Fgfr1-Related Craniosynostosis

Search GEO for disease gene expression data for Fgfr1-Related Craniosynostosis.

Pathways for Fgfr1-Related Craniosynostosis

GO Terms for Fgfr1-Related Craniosynostosis

Sources for Fgfr1-Related Craniosynostosis

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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