Preferred Name

Congenital omphalocele
Synonyms

Omphalocele

Congenital omphalocele (disorder)

Amniocele
ID

18735004
Full Id

http://purl.bioontology.org/ontology/SNOMEDCT/18735004
CONCEPTSTATUS

0
CTV3ID

XE2eb
has_associated_morphology

Congenital anomaly

Congenital protrusion

Hernial opening

Congenital failure of fusion

Hernia
has_clinical_course

Courses
has_finding_site

Umbilical structure

Intestinal structure

Abdominal wall structure
has_severity

Severities
inverse_may_be_a

Exomphalos (& congenital)

(Umbilical hernia) or (paraumbilical hernia) or (omphalocele)

Umbilical hernia (& [simple])

Umbilical hernia

Umbilical hernia (& [simple])

Exomphalos (& congenital)
inverse_was_a

Unspecified omphalocele
isa

Congenital malformation

Umbilical hernia

Intestinal hernia

Congenital anomaly of abdominal wall

Congenital anomaly of intestinal tract
ISPRIMITIVE

1
occurs_in

Congenital
same_as

Congenital omphalocele
Semantic_Type

Disease or Syndrome

Congenital Abnormality
SNOMEDID

D4-56130
SYNONYM FN

Congenital omphalocele (disorder)
SYNONYM SY

Omphalocele

Amniocele
TUI

T019

T047
UMLS_CUI

C0795690
Create New Mapping

Mapping To Ontology Source Comment Relationship Added By Added On Notes
http://purl.bioontology.org/ontology/OMIM/164750 Online Mendelian Inheritance in Man NLM UMLS (CUI) CUI: C0795690 skos:closeMatch loom 05/21/13 View Notes
http://purl.bioontology.org/ontology/MDR/10030308 MedDRA NCBO (lexical mapping) skos:closeMatch loom 05/21/13 View Notes
http://purl.bioontology.org/ontology/MDR/10030309 MedDRA NLM UMLS (CUI) CUI: C0795690 skos:closeMatch loom 05/21/13 View Notes
http://www.orphanet.org/rdfns#pat_id_551 Orphanet Ontology of Rare Diseases NCBO (lexical mapping) skos:closeMatch loom 05/21/13 View Notes
http://purl.bioontology.org/ontology/OMIM/MTHU005345 Online Mendelian Inheritance in Man NLM UMLS (CUI) CUI: C0795690 skos:closeMatch loom 05/21/13 View Notes
http://purl.bioontology.org/ontology/OMIM/164750 Online Mendelian Inheritance in Man NCBO (lexical mapping) skos:closeMatch loom 05/21/13 View Notes
http://purl.org/obo/owl/HP#HP_0001539 Bone Dysplasia Ontology NCBO (lexical mapping) skos:closeMatch loom 05/21/13 View Notes
http://purl.obolibrary.org/obo/MP_0003052 Mammalian phenotype NCBO (lexical mapping) skos:closeMatch loom 05/21/13 View Notes
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C98997 NCI Thesaurus NCBO (lexical mapping) skos:closeMatch loom 05/21/13 View Notes
http://purl.bioontology.org/ontology/ICD9CM/756.72 International Classification of Diseases NLM UMLS (CUI) CUI: C0795690 skos:closeMatch loom 05/21/13 View Notes
http://purl.bioontology.org/ontology/OMIM/MTHU005345 Online Mendelian Inheritance in Man NCBO (lexical mapping) skos:closeMatch loom 05/21/13 View Notes
http://www.semanticweb.org/ontologies/2012/11/abnormalities.owl#phenodb:1018 Fanconi Anemia (FA) Ontology NCBO (lexical mapping) skos:closeMatch loom 05/21/13 View Notes
http://purl.bioontology.org/ontology/OMIM/310980 Online Mendelian Inheritance in Man NCBO (lexical mapping) skos:closeMatch loom 05/21/13 View Notes
http://purl.bioontology.org/ontology/MDR/10030308 MedDRA NLM UMLS (CUI) CUI: C0795690 skos:closeMatch loom 05/21/13 View Notes
http://purl.bioontology.org/ontology/RCD/XE2eb Read Codes, Clinical Terms Version 3 (CTV3) NLM UMLS (CUI) CUI: C0795690 skos:closeMatch loom 05/21/13 View Notes
http://purl.bioontology.org/ontology/ICD10CM/Q79.2 ICD10CM NLM UMLS (CUI) CUI: C0795690 skos:closeMatch loom 05/21/13 View Notes
http://purl.bioontology.org/ontology/RCD/XE2eb Read Codes, Clinical Terms Version 3 (CTV3) NCBO (lexical mapping) skos:closeMatch loom 05/21/13 View Notes
http://purl.org/obo/owl/MP#MP_0003052 Suggested Ontology for Pharmacogenomics NCBO (lexical mapping) skos:closeMatch loom 05/21/13 View Notes
http://purl.bioontology.org/ontology/MSH/D006554 Medical Subject Headings (MeSH) NLM UMLS (CUI) CUI: C0795690 skos:closeMatch loom 05/21/13 View Notes
http://purl.obolibrary.org/obo/HP_0001539 Human Phenotype Ontology NCBO (lexical mapping) skos:closeMatch loom 05/21/13 View Notes
http://purl.bioontology.org/ontology/RCD/J32y0 Read Codes, Clinical Terms Version 3 (CTV3) NLM UMLS (CUI) CUI: C0795690 skos:closeMatch loom 05/21/13 View Notes
http://www.semanticweb.org/ontologies/2012/5/Ontology1338526551855.owl#Congenital_omphalocele RAPID Phenotype Ontology NCBO (lexical mapping) skos:closeMatch loom 05/21/13 View Notes
http://purl.bioontology.org/ontology/ICD9CM/756.72 International Classification of Diseases NCBO (lexical mapping) skos:closeMatch loom 05/21/13 View Notes
http://purl.bioontology.org/ontology/OMIM/310980 Online Mendelian Inheritance in Man NLM UMLS (CUI) CUI: C0795690 skos:closeMatch loom 05/21/13 View Notes

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