MCID: PRM033
MIFTS: 8

Paraomphalocele

Categories: Gastrointestinal diseases, Rare diseases

Aliases & Classifications for Paraomphalocele

MalaCards integrated aliases for Paraomphalocele:

Name: Paraomphalocele 52 71
Type - Epigastric - Defect in the Cephalic Fold 52
Type - Hypogastric - Defect in the Caudal Fold 52

Classifications:



External Ids:

UMLS 71 C2931431

Summaries for Paraomphalocele

MalaCards based summary : Paraomphalocele, also known as type - epigastric - defect in the cephalic fold, is related to gastroschisis and omphalocele. Affiliated tissues include liver.

Wikipedia : 74 Gastroschisis is a birth defect in which the baby's intestines extend outside of the abdomen through a... more...

Related Diseases for Paraomphalocele

Diseases related to Paraomphalocele via text searches within MalaCards or GeneCards Suite gene sharing:

# Related Disease Score Top Affiliating Genes
1 gastroschisis 10.2
2 omphalocele 10.2
3 abdominal wall defect 10.2

Symptoms & Phenotypes for Paraomphalocele

Drugs & Therapeutics for Paraomphalocele

Search Clinical Trials , NIH Clinical Center for Paraomphalocele

Genetic Tests for Paraomphalocele

Anatomical Context for Paraomphalocele

MalaCards organs/tissues related to Paraomphalocele:

40
Liver

Publications for Paraomphalocele

Articles related to Paraomphalocele:

# Title Authors PMID Year
1
[PARAOMPHALOCELE (SO-CALLED GASTROSCHISIS) AND OMPHALOCELE]. 61
14248924 1964

Variations for Paraomphalocele

Expression for Paraomphalocele

Search GEO for disease gene expression data for Paraomphalocele.

Pathways for Paraomphalocele

GO Terms for Paraomphalocele

Sources for Paraomphalocele

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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