MCID: DBR003
MIFTS: 9

Dobrow Syndrome

Categories: Bone diseases, Fetal diseases, Rare diseases

Aliases & Classifications for Dobrow Syndrome

MalaCards integrated aliases for Dobrow Syndrome:

Name: Dobrow Syndrome 52 58
Syngnathia-Multiple Anomalies Syndrome 58

Characteristics:

Orphanet epidemiological data:

58
dobrow syndrome
Prevalence: <1/1000000 (Worldwide);

Classifications:

Orphanet: 58  
Rare bone diseases
Developmental anomalies during embryogenesis


External Ids:

Orphanet 58 ORPHA3262

Summaries for Dobrow Syndrome

MalaCards based summary : Dobrow Syndrome, also known as syngnathia-multiple anomalies syndrome, is related to syngnathia multiple anomalies and syngnathia. Affiliated tissues include bone.

Related Diseases for Dobrow Syndrome

Diseases related to Dobrow Syndrome via text searches within MalaCards or GeneCards Suite gene sharing:

(showing 5, show less)
# Related Disease Score Top Affiliating Genes
1 syngnathia multiple anomalies 11.3
2 syngnathia 10.2
3 coloboma of macula 10.2
4 hemifacial microsomia 10.2
5 microcephaly 10.2

Graphical network of the top 20 diseases related to Dobrow Syndrome:



Diseases related to Dobrow Syndrome

Symptoms & Phenotypes for Dobrow Syndrome

Drugs & Therapeutics for Dobrow Syndrome

Search Clinical Trials , NIH Clinical Center for Dobrow Syndrome

Genetic Tests for Dobrow Syndrome

Anatomical Context for Dobrow Syndrome

MalaCards organs/tissues related to Dobrow Syndrome:

40
Bone

Publications for Dobrow Syndrome

Articles related to Dobrow Syndrome:

(showing 1, show less)
# Title Authors PMID Year
1
Bony syngnathia, vertebral segmentation defect, coloboma, microcephaly and mental retardation: confirmation of Dobrow syndrome and review of syndromal syngnathias. 61
15365455 2004

Variations for Dobrow Syndrome

Expression for Dobrow Syndrome

Search GEO for disease gene expression data for Dobrow Syndrome.

Pathways for Dobrow Syndrome

GO Terms for Dobrow Syndrome

Sources for Dobrow 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
Content
Loading form....