MCID: DWR002
MIFTS: 7

Dauwerse-Peters Syndrome

Categories: Rare diseases

Aliases & Classifications for Dauwerse-Peters Syndrome

MalaCards integrated aliases for Dauwerse-Peters Syndrome:

Name: Dauwerse-Peters Syndrome 56 52
Short Stature, Facial Dysmorphism, Severe Brachydactyly, and Syndactyly 56 71
Short Stature, Facial Dysmorphism, Severe Brachydactyly and Syndactyly 52

Classifications:



External Ids:

OMIM 56 611733
MedGen 41 C2673203
UMLS 71 C2673203

Summaries for Dauwerse-Peters Syndrome

MalaCards based summary : Dauwerse-Peters Syndrome, is also known as short stature, facial dysmorphism, severe brachydactyly, and syndactyly.

More information from OMIM: 611733

Related Diseases for Dauwerse-Peters Syndrome

Symptoms & Phenotypes for Dauwerse-Peters Syndrome

Clinical features from OMIM:

611733

Drugs & Therapeutics for Dauwerse-Peters Syndrome

Search Clinical Trials , NIH Clinical Center for Dauwerse-Peters Syndrome

Genetic Tests for Dauwerse-Peters Syndrome

Anatomical Context for Dauwerse-Peters Syndrome

Publications for Dauwerse-Peters Syndrome

Articles related to Dauwerse-Peters Syndrome:

# Title Authors PMID Year
1
A t(4;6)(q12;p23) translocation disrupts a membrane-associated O-acetyl transferase gene (MBOAT1) in a patient with a novel brachydactyly-syndactyly syndrome. 56
17440500 2007

Variations for Dauwerse-Peters Syndrome

Expression for Dauwerse-Peters Syndrome

Search GEO for disease gene expression data for Dauwerse-Peters Syndrome.

Pathways for Dauwerse-Peters Syndrome

GO Terms for Dauwerse-Peters Syndrome

Sources for Dauwerse-Peters Syndrome

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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