Preferred Name

Congenital absence of spleen
Synonyms

Splenic agenesis

Splenic aplasia

Congenital asplenia

Congenital absence of spleen (disorder)
ID

93030006
Full Id

http://purl.bioontology.org/ontology/SNOMEDCT/93030006
CONCEPTSTATUS

0
CTV3ID

XE1Mi
has_associated_morphology

Congenital absence
has_clinical_course

Courses
has_finding_site

Splenic structure
has_severity

Severities
inverse_may_be_a

(Absent spleen) or (asplenia)
isa

Congenital malformation

Congenital anomaly of spleen
ISPRIMITIVE

0
occurs_in

Congenital
Semantic_Type

Congenital Abnormality
SNOMEDID

D4-C1020
SYNONYM FN

Congenital absence of spleen (disorder)
SYNONYM SY

Splenic agenesis

Splenic aplasia

Congenital asplenia
TUI

T019
UMLS_CUI

C0600031
Create New Mapping

Mapping To Ontology Source Comment Relationship Added By Added On Notes
http://purl.bioontology.org/ontology/MDR/10053622 MedDRA NLM UMLS (CUI) CUI: C0600031 skos:closeMatch loom 04/02/13 View Notes
http://purl.bioontology.org/ontology/OMIM/MTHU009130 Online Mendelian Inheritance in Man NCBO (lexical mapping) skos:closeMatch loom 04/02/13 View Notes
http://purl.bioontology.org/ontology/OMIM/MTHU016583 Online Mendelian Inheritance in Man NCBO (lexical mapping) skos:closeMatch loom 04/02/13 View Notes
http://purl.bioontology.org/ontology/RCD/XE1Mi Read Codes, Clinical Terms Version 3 (CTV3) NLM UMLS (CUI) CUI: C0600031 skos:closeMatch loom 04/02/13 View Notes
http://purl.bioontology.org/ontology/RCD/XE1Mi Read Codes, Clinical Terms Version 3 (CTV3) NCBO (lexical mapping) skos:closeMatch loom 04/02/13 View Notes
http://purl.bioontology.org/ontology/ICD10CM/Q89.01 ICD10CM NLM UMLS (CUI) CUI: C0600031 skos:closeMatch loom 04/02/13 View Notes
http://purl.bioontology.org/ontology/OMIM/MTHU009130 Online Mendelian Inheritance in Man NLM UMLS (CUI) CUI: C0600031 skos:closeMatch loom 04/02/13 View Notes
http://purl.bioontology.org/ontology/OMIM/MTHU016583 Online Mendelian Inheritance in Man NLM UMLS (CUI) CUI: C0600031 skos:closeMatch loom 04/02/13 View Notes
http://www.semanticweb.org/ontologies/2012/5/Ontology1338526551855.owl#Congenital_absence_of_spleen RAPID Phenotype Ontology NCBO (lexical mapping) skos:closeMatch loom 04/02/13 View Notes
http://purl.bioontology.org/ontology/OMIM/MTHU011729 Online Mendelian Inheritance in Man NLM UMLS (CUI) CUI: C0600031 skos:closeMatch loom 04/02/13 View Notes

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