MCID: TRG011

Trigonocephaly, Nonsyndromic malady

Category: Genetic diseases (common)

Aliases & Classifications for Trigonocephaly, Nonsyndromic

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Aliases & Descriptions for Trigonocephaly, Nonsyndromic:

Name: Trigonocephaly, Nonsyndromic 23
 
Craniosynostosis, Metopic 23

Classifications:



Summaries for Trigonocephaly, Nonsyndromic

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MalaCards based summary: Trigonocephaly, Nonsyndromic, is also known as craniosynostosis, metopic An important gene associated with Trigonocephaly, Nonsyndromic is FGFR1 (Fibroblast Growth Factor Receptor 1). Affiliated tissues include bone.

Related Diseases for Trigonocephaly, Nonsyndromic

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Symptoms for Trigonocephaly, Nonsyndromic

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Drugs & Therapeutics for Trigonocephaly, Nonsyndromic

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Interventional clinical trials:

idNameStatusNCT IDPhase
1Comparison of a Bone Product to Bone Dust in Ossification of Small Calvarial Defects.WithdrawnNCT01006148Phase 4

Search NIH Clinical Center for Trigonocephaly, Nonsyndromic

Genetic Tests for Trigonocephaly, Nonsyndromic

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Genetic tests related to Trigonocephaly, Nonsyndromic:

id Genetic test Affiliating Genes
1 Trigonocephaly, Nonsyndromic23 FGFR1

Anatomical Context for Trigonocephaly, Nonsyndromic

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MalaCards organs/tissues related to Trigonocephaly, Nonsyndromic:

34
Bone

Animal Models for Trigonocephaly, Nonsyndromic or affiliated genes

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Publications for Trigonocephaly, Nonsyndromic

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Variations for Trigonocephaly, Nonsyndromic

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Expression for genes affiliated with Trigonocephaly, Nonsyndromic

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Search GEO for disease gene expression data for Trigonocephaly, Nonsyndromic.

Pathways for genes affiliated with Trigonocephaly, Nonsyndromic

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GO Terms for genes affiliated with Trigonocephaly, Nonsyndromic

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Sources for Trigonocephaly, Nonsyndromic

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2CDC
6CNVD
10DGIdb
15ExPASy
16FDA
17FMA
25GTR
26HGMD
27HMDB
28ICD10
29ICD10 via Orphanet
30ICD9CM
31IUPHAR
32KEGG
35MedGen
37MeSH
38MESH via Orphanet
39MGI
42NCI
43NCIt
44NDF-RT
47NINDS
48Novoseek
50OMIM
51OMIM via Orphanet
55PubMed
56QIAGEN
61SNOMED-CT via Orphanet
65Tumor Gene Family of Databases
66UMLS
67UMLS via Orphanet