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 52

Classifications:



Summaries for Syngnathia Multiple Anomalies

NIH Rare Diseases : 52 The following summary is from Orphanet , a European reference portal for information on rare diseases and orphan drugs. Orpha Number: 3262 Definition Dobrow 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:

(showing 1, show less)
# 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 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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