MCID: VNG001
MIFTS: 12

Vangl1-Related Neural Tube Defect malady

Categories: Genetic diseases

Aliases & Classifications for Vangl1-Related Neural Tube Defect

Aliases & Descriptions for Vangl1-Related Neural Tube Defect:

Name: Vangl1-Related Neural Tube Defect 24
Vangl1-Related Ntd 24
Spina Bifida 24
Anencephaly 24

Classifications:



Summaries for Vangl1-Related Neural Tube Defect

MalaCards based summary : Vangl1-Related Neural Tube Defect, also known as vangl1-related ntd, is related to spina bifida occulta and neural tube defects. An important gene associated with Vangl1-Related Neural Tube Defect is VANGL1 (VANGL Planar Cell Polarity Protein 1).

Related Diseases for Vangl1-Related Neural Tube Defect

Diseases related to Vangl1-Related Neural Tube Defect via text searches within MalaCards or GeneCards Suite gene sharing:

(show top 50) (show all 145)
id Related Disease Score Top Affiliating Genes
1 spina bifida occulta 12.6
2 neural tube defects 12.5
3 spina bifida aperta 12.3
4 spina bifida hypospadias 12.2
5 cervical spina bifida cystica 12.1
6 lumbosacral spina bifida cystica 12.1
7 split-hand with obstructive uropathy, spina bifida, and diaphragmatic defects 12.1
8 anencephaly and spina bifida x-linked 12.1
9 cervical spina bifida aperta 12.0
10 split hand urinary anomalies spina bifida 12.0
11 myelomeningocele 12.0
12 thoracolumbosacral spina bifida aperta 12.0
13 lumbosacral spina bifida aperta 12.0
14 cervicothoracic spina bifida aperta 12.0
15 total spina bifida aperta 12.0
16 upper thoracic spina bifida cystica 12.0
17 cervicothoracic spina bifida cystica 12.0
18 thoracolumbosacral spina bifida cystica 12.0
19 total spina bifida cystica 12.0
20 upper thoracic spina bifida aperta 12.0
21 neural tube defects, folate-sensitive 11.8
22 tethered spinal cord syndrome 11.5
23 encephalocele 11.5
24 hydrocephalus 11.4
25 tethered cord syndrome 11.4
26 caudal regression syndrome 11.4
27 chiari malformation 11.4
28 craniorachischisis 11.3
29 chiari malformation type ii 11.2
30 kasznica carlson coppedge syndrome 11.2
31 iniencephaly 11.2
32 myelocystocele 11.1
33 spinal disease 11.0
34 absence of gluteal muscle 11.0
35 acrodysplasia scoliosis 11.0
36 omphalocele, exstrophy of the cloaca, imperforate anus, and spinal defects complex 11.0
37 basal cell nevus syndrome 11.0
38 congenital laryngeal palsy 11.0
39 anencephaly 10.8
40 cerebritis 10.4
41 neurogenic bladder 10.3
42 meningocele 10.3
43 lipomyelomeningocele 10.2
44 cervicitis 10.2
45 cerebral palsy 10.2
46 spinal cord injury 10.2
47 latex allergy 10.1
48 birth defects 10.1
49 spondylolisthesis 10.1
50 fecal incontinence 10.1

Graphical network of the top 20 diseases related to Vangl1-Related Neural Tube Defect:



Diseases related to Vangl1-Related Neural Tube Defect

Symptoms & Phenotypes for Vangl1-Related Neural Tube Defect

Drugs & Therapeutics for Vangl1-Related Neural Tube Defect

Search Clinical Trials , NIH Clinical Center for Vangl1-Related Neural Tube Defect

Genetic Tests for Vangl1-Related Neural Tube Defect

Genetic tests related to Vangl1-Related Neural Tube Defect:

id Genetic test Affiliating Genes
1 Vangl1-Related Neural Tube Defect 24 VANGL1

Anatomical Context for Vangl1-Related Neural Tube Defect

Publications for Vangl1-Related Neural Tube Defect

Variations for Vangl1-Related Neural Tube Defect

ClinVar genetic disease variations for Vangl1-Related Neural Tube Defect:

6
id Gene Variation Type Significance SNP ID Assembly Location
1 CCL2 NG_012123.1: g.2493A> G single nucleotide variant Pathogenic,risk factor rs1024611 GRCh37 Chromosome 17, 32579788: 32579788

Expression for Vangl1-Related Neural Tube Defect

Search GEO for disease gene expression data for Vangl1-Related Neural Tube Defect.

Pathways for Vangl1-Related Neural Tube Defect

GO Terms for Vangl1-Related Neural Tube Defect

Sources for Vangl1-Related Neural Tube Defect

3 CDC
7 CNVD
9 Cosmic
10 dbSNP
11 DGIdb
16 ExPASy
18 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 MedGen
42 MeSH
43 MESH via Orphanet
44 MGI
46 NCI
47 NCIt
48 NDF-RT
51 NINDS
52 Novoseek
54 OMIM
55 OMIM via Orphanet
59 PubMed
60 QIAGEN
65 SNOMED-CT via Orphanet
67 TGDB
68 Tocris
69 UMLS
70 UMLS via Orphanet
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