Aliases & Classifications for Fg Syndrome 5

MalaCards integrated aliases for Fg Syndrome 5:

Name: Fg Syndrome 5 57 29 13 70
Fgs5 57

External Ids:

OMIM® 57 300581
OMIM Phenotypic Series 57 PS305400
MedGen 41 C1845119
UMLS 70 C1845119

Summaries for Fg Syndrome 5

MalaCards based summary : Fg Syndrome 5, also known as fgs5, is related to opitz-kaveggia syndrome and opitz-gbbb syndrome, and has symptoms including constipation An important gene associated with Fg Syndrome 5 is FGS5 (FG Syndrome 5).

More information from OMIM: 300581 PS305400

Related Diseases for Fg Syndrome 5

Diseases related to Fg Syndrome 5 via text searches within MalaCards or GeneCards Suite gene sharing:

# Related Disease Score Top Affiliating Genes
1 opitz-kaveggia syndrome 9.9
2 opitz-gbbb syndrome 9.9
3 med12-related disorders 9.9

Symptoms & Phenotypes for Fg Syndrome 5

Clinical features from OMIM®:

300581 (Updated 05-Apr-2021)

UMLS symptoms related to Fg Syndrome 5:


constipation

Drugs & Therapeutics for Fg Syndrome 5

Search Clinical Trials , NIH Clinical Center for Fg Syndrome 5

Genetic Tests for Fg Syndrome 5

Genetic tests related to Fg Syndrome 5:

# Genetic test Affiliating Genes
1 Fg Syndrome 5 29

Anatomical Context for Fg Syndrome 5

Publications for Fg Syndrome 5

Articles related to Fg Syndrome 5:

# Title Authors PMID Year
1
An Xq22.3 duplication detected by comparative genomic hybridization microarray (Array-CGH) defines a new locus (FGS5) for FG syndrome. 57 61
16283679 2005
2
A male infant with Xq22.2q22.3 duplication containing PLP1 and MID2. 61
31951325 2020

Variations for Fg Syndrome 5

Expression for Fg Syndrome 5

Search GEO for disease gene expression data for Fg Syndrome 5.

Pathways for Fg Syndrome 5

GO Terms for Fg Syndrome 5

Sources for Fg Syndrome 5

3 CDC
7 CNVD
9 Cosmic
10 dbSNP
11 DGIdb
17 EFO
18 ExPASy
19 FMA
20 GARD
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
44 MeSH
45 MESH via Orphanet
46 MGI
49 NCI
50 NCIt
51 NDF-RT
53 NINDS
54 Novoseek
56 OMIM via Orphanet
57 OMIM® (Updated 05-Apr-2021)
61 PubMed
63 QIAGEN
68 SNOMED-CT via HPO
69 Tocris
70 UMLS
71 UMLS via Orphanet
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