MCID: CRN299
MIFTS: 7

Craniosynostosis Syndrome, Autosomal Recessive

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

Aliases & Classifications for Craniosynostosis Syndrome, Autosomal Recessive

MalaCards integrated aliases for Craniosynostosis Syndrome, Autosomal Recessive:

Name: Craniosynostosis Syndrome, Autosomal Recessive 56

Classifications:



External Ids:

OMIM 56 606529
MedGen 41 C1847865

Summaries for Craniosynostosis Syndrome, Autosomal Recessive

MalaCards based summary : Craniosynostosis Syndrome, Autosomal Recessive

More information from OMIM: 606529

Related Diseases for Craniosynostosis Syndrome, Autosomal Recessive

Symptoms & Phenotypes for Craniosynostosis Syndrome, Autosomal Recessive

Clinical features from OMIM:

606529

Drugs & Therapeutics for Craniosynostosis Syndrome, Autosomal Recessive

Search Clinical Trials , NIH Clinical Center for Craniosynostosis Syndrome, Autosomal Recessive

Genetic Tests for Craniosynostosis Syndrome, Autosomal Recessive

Anatomical Context for Craniosynostosis Syndrome, Autosomal Recessive

Publications for Craniosynostosis Syndrome, Autosomal Recessive

Articles related to Craniosynostosis Syndrome, Autosomal Recessive:

(showing 1, show less)
# Title Authors PMID Year
1
Newly recognised craniosynostosis syndrome that does not map to known disease loci. 56
11074486 2000

Variations for Craniosynostosis Syndrome, Autosomal Recessive

Expression for Craniosynostosis Syndrome, Autosomal Recessive

Search GEO for disease gene expression data for Craniosynostosis Syndrome, Autosomal Recessive.

Pathways for Craniosynostosis Syndrome, Autosomal Recessive

GO Terms for Craniosynostosis Syndrome, Autosomal Recessive

Sources for Craniosynostosis Syndrome, Autosomal Recessive

3 CDC
7 CNVD
9 Cosmic
10 dbSNP
11 DGIdb
17 EFO
18 ExPASy
19 FMA
28 GO
29 GTR
30 HMDB
31 HPO
32 ICD10
33 ICD10 via Orphanet
34 ICD9CM
35 IUPHAR
36 KEGG
37 LifeMap
39 LOVD
41 MedGen
43 MeSH
44 MESH via Orphanet
45 MGI
48 NCI
49 NCIt
50 NDF-RT
53 NINDS
54 Novoseek
56 OMIM
57 OMIM via Orphanet
61 PubMed
63 QIAGEN
68 SNOMED-CT via HPO
69 TGDB
70 Tocris
71 UMLS
72 UMLS via Orphanet
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