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702624008: Aplasia of spleen (disorder)


Status: current, Sufficiently defined by necessary conditions definition status. Date: 31-Jul 2014. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
3005254019 Aplasia of spleen (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
3005263017 Aplasia of spleen en Synonym Active Entire term case insensitive SNOMED CT core module
3005336016 Splenic aplasia en Synonym Active Entire term case insensitive SNOMED CT core module


1 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Aplasia of spleen Is a Congenital anomaly of spleen true Inferred relationship Existential restriction modifier
Aplasia of spleen Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Aplasia of spleen Associated morphology Aplasia true Inferred relationship Existential restriction modifier 1
Aplasia of spleen Finding site Splenic structure true Inferred relationship Existential restriction modifier 1
Aplasia of spleen Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1

Inbound Relationships Type Active Source Characteristic Refinability Group
Congenital absence of spleen Is a False Aplasia of spleen Inferred relationship Existential restriction modifier
Familial isolated congenital asplenia Is a False Aplasia of spleen Inferred relationship Existential restriction modifier
Bilateral right-sidedness sequence Is a False Aplasia of spleen Inferred relationship Existential restriction modifier
Agenesis of spleen Is a True Aplasia of spleen Inferred relationship Existential restriction modifier

This concept is not in any reference sets

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