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205735005: Hypoplasia of spleen (disorder)

Status: current, Sufficiently defined by necessary conditions definition status. Date: 31-Jan 2013. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
315505011 Hypoplasia of spleen en Synonym Active Entire term case insensitive SNOMED CT core module
591143011 Hypoplasia of spleen (disorder) en Fully specified name 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
Hypoplasia of spleen Is a Congenital anomaly of spleen false Inferred relationship Existential restriction modifier
Hypoplasia of spleen Finding site Splenic structure false Inferred relationship Existential restriction modifier 1
Hypoplasia of spleen Occurrence Congenital false Inferred relationship Existential restriction modifier
Hypoplasia of spleen Finding site Structure of digestive system false Inferred relationship Existential restriction modifier 1
Hypoplasia of spleen Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier 1
Hypoplasia of spleen Finding site Splenic structure false Inferred relationship Existential restriction modifier 1
Hypoplasia of spleen Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier 1
Hypoplasia of spleen Associated morphology Hypoplasia true Inferred relationship Existential restriction modifier 2
Hypoplasia of spleen Is a Disorder of spleen true Inferred relationship Existential restriction modifier
Hypoplasia of spleen Finding site Splenic structure true Inferred relationship Existential restriction modifier 2
Inbound Relationships Type Active Source Characteristic Refinability Group
Congenital hypoplasia of spleen Is a True Hypoplasia of spleen Inferred relationship Existential restriction modifier

This concept is not in any reference sets

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