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93292008: Congenital hypoplasia of spleen (disorder)


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

Descriptions:

Id Description Lang Type Status Case? Module
154381013 Congenital hypoplasia of spleen en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
154382018 Congenital microsplenia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
154383011 Congenital small spleen en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
836995018 Congenital hypoplasia of spleen (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
154381013 Congenital hypoplasia of spleen en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
154381013 Congenital hypoplasia of spleen en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
154382018 Congenital microsplenia en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
154382018 Congenital microsplenia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
154383011 Congenital small spleen en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
154383011 Congenital small spleen en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
836995018 Congenital hypoplasia of spleen (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
836995018 Congenital hypoplasia of spleen (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
4709311000241115 hypoplasie splénique congénitale fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
4709311000241115 hypoplasie splénique congénitale fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Congenital hypoplasia of spleen Is a Congenital anomaly of spleen true Inferred relationship Existential restriction modifier (core metadata concept)
Congenital hypoplasia of spleen Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital hypoplasia of spleen Associated morphology Congenital hypoplasia false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital hypoplasia of spleen Finding site Splenic structure false Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital hypoplasia of spleen Finding site Structure of digestive system (body structure) false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital hypoplasia of spleen Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital hypoplasia of spleen Is a Congenital malformation false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital hypoplasia of spleen Is a Congenital anomaly of digestive system false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital hypoplasia of spleen Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital hypoplasia of spleen Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital hypoplasia of spleen Finding site Splenic structure false Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital hypoplasia of spleen Finding site Structure of digestive system (body structure) false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital hypoplasia of spleen Associated morphology Congenital hypoplasia false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital hypoplasia of spleen Associated morphology Congenital hypoplasia false Inferred relationship Existential restriction modifier (core metadata concept) 3
Congenital hypoplasia of spleen Is a Hypoplasia of spleen (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Congenital hypoplasia of spleen Finding site Splenic structure false Inferred relationship Existential restriction modifier (core metadata concept) 3
Congenital hypoplasia of spleen Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital hypoplasia of spleen Finding site Splenic structure true Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital hypoplasia of spleen Associated morphology Hypoplasia true Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital hypoplasia of spleen Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 1

Inbound Relationships Type Active Source Characteristic Refinability Group
Hereditary splenic hypoplasia Is a False Congenital hypoplasia of spleen Inferred relationship Existential restriction modifier (core metadata concept)

This concept is not in any reference sets

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