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Omphalocele
MeSH Descriptor Data 2026
Details
Qualifiers
MeSH Tree Structures
Concepts
MeSH Heading
Omphalocele
Tree Number(s)
C16.131.703
Unique ID
D000099245
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/D000099245
Scope Note
A congenital defect with major fissure in the
ABDOMINAL WALL
at the
UMBILICUS
resulting in the extrusion of
VISCERA
through the
UMBILICUS
. Unlike
GASTROSCHISIS
, omphalocele is covered with
PERITONEUM
but without overlying
SKIN
.
Entry Term(s)
Exomphalos
Previous Indexing
HERNIA, UMBILICAL (1980-2025)
Public MeSH Note
2026; see HERNIA, UMBILICAL 1980-2025, see UMBILICAL HERNIA 1963-1979
History Note
2026; use HERNIA, UMBILICAL 1980-2025
Date Introduced
2026/01/01
Last Updated
2026/01/01
Allowable Qualifiers
blood (BL)
cerebrospinal fluid (CF)
chemically induced (CI)
classification (CL)
complications (CO)
diagnosis (DI)
diagnostic imaging (DG)
diet therapy (DH)
drug therapy (DT)
economics (EC)
embryology (EM)
enzymology (EN)
epidemiology (EP)
ethnology (EH)
etiology (ET)
genetics (GE)
history (HI)
immunology (IM)
metabolism (ME)
microbiology (MI)
mortality (MO)
nursing (NU)
parasitology (PS)
pathology (PA)
physiopathology (PP)
prevention & control (PC)
psychology (PX)
radiotherapy (RT)
rehabilitation (RH)
surgery (SU)
therapy (TH)
urine (UR)
veterinary (VE)
virology (VI)
Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
Congenital Abnormalities [C16.131]
Abnormalities, Drug-Induced [C16.131.042]
Abnormalities, Multiple [C16.131.077]
Abnormalities, Radiation-Induced [C16.131.080]
Abnormalities, Severe Teratoid [C16.131.085]
Aicardi Syndrome [C16.131.162]
Cardiovascular Abnormalities [C16.131.240]
Chromosome Disorders [C16.131.260]
Congenital Microtia [C16.131.287]
Digestive System Abnormalities [C16.131.314]
Eye Abnormalities [C16.131.384]
Hernias, Diaphragmatic, Congenital [C16.131.433]
Lymphatic Abnormalities [C16.131.482]
Musculoskeletal Abnormalities [C16.131.621]
Nervous System Malformations [C16.131.666]
Omphalocele [C16.131.703]
Respiratory System Abnormalities [C16.131.740]
Situs Inversus [C16.131.810]
Skin Abnormalities [C16.131.831]
Stomatognathic System Abnormalities [C16.131.850]
Thyroid Dysgenesis [C16.131.894]
Urogenital Abnormalities [C16.131.939]
Expand All
Collapse All
Omphalocele
Preferred
Concept UI
M0010270
Scope Note
A congenital defect with major fissure in the
ABDOMINAL WALL
at the
UMBILICUS
resulting in the extrusion of
VISCERA
through the
UMBILICUS
. Unlike
GASTROSCHISIS
, omphalocele is covered with
PERITONEUM
but without overlying
SKIN
.
Terms
Omphalocele
Preferred Term
Term UI
T019743
Date
12/31/1976
LexicalTag
NON
ThesaurusID
Exomphalos
Narrower
Concept UI
M000769018
Terms
Exomphalos
Preferred Term
Term UI
T019740
Date
12/31/1976
LexicalTag
NON
ThesaurusID
UNK (19XX)
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