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Diseases

Congenital omphalocele

congenital omphalocele

Entity Type
Diseases
Relation Groups
3
Relation Preview
24

Basic Information

Grouped by core information, identifiers, and descriptions.

Current candidates are inferred from disease-target-ingredient-herb paths and do not represent a formal recommendation ranking.

Core Information

Disease Name
Congenital omphalocele
Standard Disease Name
congenital omphalocele
MeSH Tree
No data
ICD-10
No data

Identifiers

DO ID
No data
MeSH ID
No data
OMIM ID
No data
UMLS ID
No data
HPO ID
No data

Description and Extensions

Description
No data
Related

Direct relations and traceable candidates grouped by relation type.

Related Targets

target disease8 Targets
02
CHUK
component of inhibitor of nuclear factor kappa B kinase complex
component of inhibitor of nuclear factor kappa B kinase complex
04
GYPB
glycophorin B (MNS blood group)
glycophorin B (MNS blood group)
06
KCNQ1
potassium voltage-gated channel subfamily Q member 1
potassium voltage-gated channel subfamily Q member 1
08
PAFAH1B1
platelet activating factor acetylhydrolase 1b regulatory subunit 1
platelet activating factor acetylhydrolase 1b regulatory subunit 1