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 57

Classifications:



External Ids:

OMIM 57 606529
MedGen 42 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:

# Title Authors PMID Year
1
Newly recognised craniosynostosis syndrome that does not map to known disease loci. 8
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 HGMD
31 HMDB
32 HPO
33 ICD10
34 ICD10 via Orphanet
35 ICD9CM
36 IUPHAR
37 KEGG
38 LifeMap
40 LOVD
42 MedGen
44 MeSH
45 MESH via Orphanet
46 MGI
49 NCI
50 NCIt
51 NDF-RT
54 NINDS
55 Novoseek
57 OMIM
58 OMIM via Orphanet
62 PubMed
64 QIAGEN
69 SNOMED-CT via HPO
70 TGDB
71 Tocris
72 UMLS
73 UMLS via Orphanet
Content
Loading form....