MCID: FGS003
MIFTS: 8

Fg Syndrome 3

Categories: Rare diseases

Aliases & Classifications for Fg Syndrome 3

MalaCards integrated aliases for Fg Syndrome 3:

Name: Fg Syndrome 3 57 53 13 73
Fgs3 57 53

Classifications:



External Ids:

OMIM 57 300406
UMLS 73 C1845567

Summaries for Fg Syndrome 3

MalaCards based summary : Fg Syndrome 3, also known as fgs3, is related to opitz-kaveggia syndrome. An important gene associated with Fg Syndrome 3 is FGS3 (FG Syndrome 3).

Description from OMIM: 300406

Related Diseases for Fg Syndrome 3

Diseases related to Fg Syndrome 3 via text searches within MalaCards or GeneCards Suite gene sharing:

# Related Disease Score Top Affiliating Genes
1 opitz-kaveggia syndrome 11.3

Symptoms & Phenotypes for Fg Syndrome 3

Clinical features from OMIM:

300406

Drugs & Therapeutics for Fg Syndrome 3

Search Clinical Trials , NIH Clinical Center for Fg Syndrome 3

Genetic Tests for Fg Syndrome 3

Anatomical Context for Fg Syndrome 3

Publications for Fg Syndrome 3

Variations for Fg Syndrome 3

Expression for Fg Syndrome 3

Search GEO for disease gene expression data for Fg Syndrome 3.

Pathways for Fg Syndrome 3

GO Terms for Fg Syndrome 3

Sources for Fg Syndrome 3

3 CDC
7 CNVD
9 Cosmic
10 dbSNP
11 DGIdb
17 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 SNOMED-CT via Orphanet
71 TGDB
72 Tocris
73 UMLS
74 UMLS via Orphanet
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