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 53 59
Syngnathia-Multiple Anomalies Syndrome 59

Characteristics:

Orphanet epidemiological data:

59
dobrow syndrome
Prevalence: <1/1000000 (Worldwide);

Classifications:



External Ids:

Orphanet 59 ORPHA3262

Summaries for Dobrow Syndrome

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

Related Diseases for Dobrow Syndrome

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

# Related Disease Score Top Affiliating Genes
1 syngnathia 10.2
2 coloboma of macula 10.2
3 hemifacial microsomia 10.2
4 microcephaly 10.2

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:

41
Bone

Publications for Dobrow Syndrome

Articles related to Dobrow Syndrome:

# Title Authors PMID Year
1
Bony syngnathia, vertebral segmentation defect, coloboma, microcephaly and mental retardation: confirmation of Dobrow syndrome and review of syndromal syngnathias. 38
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 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
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