FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.10  |  FHIR Version n/a  User: [n/a]

93030006: Congenital absence of spleen (disorder)


Status: current, Sufficiently defined by necessary conditions definition status. Date: 31-Jan 2002. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
153877013 Congenital absence of spleen en Synonym Active Entire term case insensitive SNOMED CT core module
153878015 Congenital asplenia en Synonym Active Entire term case insensitive SNOMED CT core module
836678011 Congenital absence of spleen (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module


3 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Congenital absence of spleen Is a Congenital anomaly of spleen true Inferred relationship Existential restriction modifier
Congenital absence of spleen Finding site Splenic structure false Inferred relationship Existential restriction modifier 2
Congenital absence of spleen Occurrence Congenital false Inferred relationship Existential restriction modifier
Congenital absence of spleen Associated morphology Congenital absence false Inferred relationship Existential restriction modifier 1
Congenital absence of spleen Finding site Structure of digestive system false Inferred relationship Existential restriction modifier 1
Congenital absence of spleen Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier 1
Congenital absence of spleen Is a Congenital malformation false Inferred relationship Existential restriction modifier
Congenital absence of spleen Is a Congenital anomaly of digestive system false Inferred relationship Existential restriction modifier
Congenital absence of spleen Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier 2
Congenital absence of spleen Associated morphology Congenital absence false Inferred relationship Existential restriction modifier 1
Congenital absence of spleen Finding site Splenic structure false Inferred relationship Existential restriction modifier 1
Congenital absence of spleen Associated morphology Congenital absence false Inferred relationship Existential restriction modifier 1
Congenital absence of spleen Finding site Splenic structure true Inferred relationship Existential restriction modifier 1
Congenital absence of spleen Occurrence Congenital false Inferred relationship Existential restriction modifier 2
Congenital absence of spleen Finding site Splenic structure false Inferred relationship Existential restriction modifier 2
Congenital absence of spleen Is a Aplasia of spleen false Inferred relationship Existential restriction modifier
Congenital absence of spleen Is a Congenital absence false Inferred relationship Existential restriction modifier
Congenital absence of spleen Associated morphology Congenital absence false Inferred relationship Existential restriction modifier 2
Congenital absence of spleen Is a Asplenia true Inferred relationship Existential restriction modifier
Congenital absence of spleen Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Congenital absence of spleen Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Congenital absence of spleen Associated morphology Agenesis false Inferred relationship Existential restriction modifier 1
Congenital absence of spleen Finding site Entire spleen false Inferred relationship Existential restriction modifier 1
Congenital absence of spleen Associated morphology Absence true Inferred relationship Existential restriction modifier 1

Inbound Relationships Type Active Source Characteristic Refinability Group
Functional asplenia Is a False Congenital absence of spleen Inferred relationship Existential restriction modifier
Bilateral right-sidedness sequence Is a False Congenital absence of spleen Inferred relationship Existential restriction modifier
Familial isolated congenital asplenia Is a True Congenital absence of spleen Inferred relationship Existential restriction modifier
Agenesis of spleen Is a True Congenital absence of spleen Inferred relationship Existential restriction modifier
Diaphragmatic hernia, short bowel, asplenia syndrome Is a True Congenital absence of spleen Inferred relationship Existential restriction modifier

This concept is not in any reference sets

Back to Start