MCID: SYN028
MIFTS: 3

Syngnathia Multiple Anomalies

Categories: Fetal diseases, Rare diseases

Aliases & Classifications for Syngnathia Multiple Anomalies

MalaCards integrated aliases for Syngnathia Multiple Anomalies:

Name: Syngnathia Multiple Anomalies 53

Classifications:



Summaries for Syngnathia Multiple Anomalies

NIH Rare Diseases : 53 The following summary is from Orphanet, a European reference portal for information on rare diseases and orphan drugs.Orpha Number: 3262DefinitionDobrow syndrome is a rare multiple congenital defects/dysmorphic syndrome characterized by variable degrees of bony syngnathia associated with variable additional abnormalities, including growth retardation, intellectual disability, microcephaly, iris coloboma, nystagmus, deafness, and vertebral segmentation defects, as well as genital, limb and additional facial malformations, among others.Visit the Orphanet disease page for more resources.

MalaCards based summary : Syngnathia Multiple Anomalies is related to dobrow syndrome.

Related Diseases for Syngnathia Multiple Anomalies

Diseases in the Syngnathia family:

Syngnathia Multiple Anomalies

Diseases related to Syngnathia Multiple Anomalies via text searches within MalaCards or GeneCards Suite gene sharing:

# Related Disease Score Top Affiliating Genes
1 dobrow syndrome 11.5

Symptoms & Phenotypes for Syngnathia Multiple Anomalies

Drugs & Therapeutics for Syngnathia Multiple Anomalies

Search Clinical Trials , NIH Clinical Center for Syngnathia Multiple Anomalies

Genetic Tests for Syngnathia Multiple Anomalies

Anatomical Context for Syngnathia Multiple Anomalies

Publications for Syngnathia Multiple Anomalies

Variations for Syngnathia Multiple Anomalies

Expression for Syngnathia Multiple Anomalies

Search GEO for disease gene expression data for Syngnathia Multiple Anomalies.

Pathways for Syngnathia Multiple Anomalies

GO Terms for Syngnathia Multiple Anomalies

Sources for Syngnathia Multiple Anomalies

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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