MCID: FGF007
MIFTS: 15

Fgfr3-Related Craniosynostosis malady

Genetic diseases, Bone diseases, Fetal diseases, Rare diseases categories

Aliases & Classifications for Fgfr3-Related Craniosynostosis

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Aliases & Descriptions for Fgfr3-Related Craniosynostosis:

Name: Fgfr3-Related Craniosynostosis 22


Classifications:



Summaries for Fgfr3-Related Craniosynostosis

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MalaCards based summary: Fgfr3-Related Craniosynostosis is related to muenke syndrome and craniosynostosis. An important gene associated with Fgfr3-Related Craniosynostosis is FGFR3 (Fibroblast Growth Factor Receptor 3). Affiliated tissues include bone.

Related Diseases for Fgfr3-Related Craniosynostosis

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Diseases in the Craniosynostosis family:

Craniosynostosis 6 Craniosynostosis, Type 2
Craniosynostosis, Type 1 Craniosynostosis 5
Craniosynostosis 3 Craniosynostosis 4
Craniosynostosis Autosomal Dominant Craniosynostosis, Nonsyndromic
Erf-Related Craniosynostosis Fgfr1-Related Craniosynostosis
Fgfr2-Related Craniosynostosis fgfr3-related craniosynostosis
Msx2-Related Craniosynostosis Tcf12-Related Craniosynostosis
Twist1-Related Craniosynostosis

Diseases related to Fgfr3-Related Craniosynostosis via text searches within MalaCards or GeneCards Suite gene sharing:

(show all 35)
idRelated DiseaseScoreTop Affiliating Genes
1muenke syndrome10.6
2craniosynostosis10.5
3adult syndrome10.2
4craniosynostosis, type 110.2
5craniosynostosis and dental anomalies10.2
6fanconi anemia, complementation group c10.2
7crouzon syndrome10.2
8craniosynostosis 310.2
9image syndrome10.2
10child syndrome10.2
11human venous malformation10.2
12pharyngitis10.2
13sensorineural hearing loss10.2
14secondary syphilis10.2
15auditory system disease10.2
16bone development disease10.2
17bone structure disease10.2
18dysostosis10.2
19globe disease10.2
20inner ear disease10.2
21labyrinthine disease10.2
22middle ear disease10.2
23nose disease10.2
24synostosis10.2
25vein disease10.2
26genetic brain disorders10.2
27head and brain malformations10.2
28hearing disorders and deafness10.2
29hearing problems in children10.2
30deafness and hereditary hearing loss10.2
31deafness craniofacial syndrome10.2
32familial deafness10.2
33kid syndrome10.2
34plagiocephaly10.2
35hearing loss/deafness10.2

Graphical network of the top 20 diseases related to Fgfr3-Related Craniosynostosis:



Diseases related to fgfr3-related craniosynostosis

Symptoms for Fgfr3-Related Craniosynostosis

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Drugs & Therapeutics for Fgfr3-Related Craniosynostosis

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Interventional clinical trials:

idNameStatusNCT IDPhase
1Clinical Study of Muenke Syndrome (FGFR3-Related Craniosynostosis)RecruitingNCT00106977

Search NIH Clinical Center for Fgfr3-Related Craniosynostosis

Genetic Tests for Fgfr3-Related Craniosynostosis

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Genetic tests related to Fgfr3-Related Craniosynostosis:

id Genetic test Affiliating Genes
1 Fgfr3-Related Craniosynostosis22 FGFR3

Anatomical Context for Fgfr3-Related Craniosynostosis

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MalaCards organs/tissues related to Fgfr3-Related Craniosynostosis:

33
Bone

Animal Models for Fgfr3-Related Craniosynostosis or affiliated genes

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Publications for Fgfr3-Related Craniosynostosis

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Articles related to Fgfr3-Related Craniosynostosis:

idTitleAuthorsYear
1
Palatal and oral manifestations of Muenke syndrome (FGFR3-related craniosynostosis). (22565872)
2012
2
Epilepsy in Muenke syndrome: FGFR3-related craniosynostosis. (23044018)
2012
3
Muenke syndrome (FGFR3-related craniosynostosis): expansion of the phenotype and review of the literature. (18000976)
2007

Variations for Fgfr3-Related Craniosynostosis

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Expression for genes affiliated with Fgfr3-Related Craniosynostosis

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Search GEO for disease gene expression data for Fgfr3-Related Craniosynostosis.

Pathways for genes affiliated with Fgfr3-Related Craniosynostosis

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GO Terms for genes affiliated with Fgfr3-Related Craniosynostosis

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Sources for Fgfr3-Related Craniosynostosis

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2CDC
14ExPASy
15FDA
16FMA
24GTR
25HGMD
26HMDB
27ICD10
28ICD10 via Orphanet
29ICD9CM
30IUPHAR
31KEGG
34MedGen
36MeSH
37MESH via Orphanet
38MGI
41NCI
42NCIt
43NDF-RT
46NINDS
47Novoseek
49OMIM
50OMIM via Orphanet
54PubMed
55QIAGEN
60SNOMED-CT via Orphanet
64Tumor Gene Family of Databases
65UMLS
66UMLS via Orphanet