FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.24  |  FHIR Version n/a  User: [n/a]

93292008: Congenital hypoplasia 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
154381013 Congenital hypoplasia of spleen en Synonym Active Entire term case insensitive SNOMED CT core module
154382018 Congenital microsplenia en Synonym Active Entire term case insensitive SNOMED CT core module
154383011 Congenital small spleen en Synonym Active Entire term case insensitive SNOMED CT core module
836995018 Congenital hypoplasia of spleen (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core 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
Congenital hypoplasia of spleen Occurrence Congenital false Inferred relationship Existential restriction modifier
Congenital hypoplasia of spleen Associated morphology Congenital hypoplasia false Inferred relationship Existential restriction modifier 1
Congenital hypoplasia of spleen Finding site Splenic structure false Inferred relationship Existential restriction modifier 2
Congenital hypoplasia of spleen Finding site Structure of digestive system false Inferred relationship Existential restriction modifier 1
Congenital hypoplasia of spleen Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier 1
Congenital hypoplasia of spleen Is a Congenital malformation false Inferred relationship Existential restriction modifier
Congenital hypoplasia of spleen Is a Congenital anomaly of digestive system false Inferred relationship Existential restriction modifier
Congenital hypoplasia of spleen Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier 2
Congenital hypoplasia of spleen Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier 2
Congenital hypoplasia of spleen Finding site Splenic structure false Inferred relationship Existential restriction modifier 2
Congenital hypoplasia of spleen Finding site Structure of digestive system false Inferred relationship Existential restriction modifier 1
Congenital hypoplasia of spleen Associated morphology Congenital hypoplasia false Inferred relationship Existential restriction modifier 1
Congenital hypoplasia of spleen Associated morphology Congenital hypoplasia false Inferred relationship Existential restriction modifier 3
Congenital hypoplasia of spleen Is a Hypoplasia of spleen true Inferred relationship Existential restriction modifier
Congenital hypoplasia of spleen Finding site Splenic structure false Inferred relationship Existential restriction modifier 3
Congenital hypoplasia of spleen Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Congenital hypoplasia of spleen Finding site Splenic structure true Inferred relationship Existential restriction modifier 1
Congenital hypoplasia of spleen Associated morphology Hypoplasia true Inferred relationship Existential restriction modifier 1
Congenital hypoplasia of spleen Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1

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

This concept is not in any reference sets

Back to Start