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80378000: Neonatal hepatosplenomegaly (disorder)


Status: current, Sufficiently defined by necessary conditions definition status. Date: 31-Jan 2005. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
133378017 Neonatal hepatosplenomegaly en Synonym Active Entire term case insensitive SNOMED CT core module
821531011 Neonatal hepatosplenomegaly (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
Neonatal hepatosplenomegaly Is a Hepatosplenomegaly true Inferred relationship Existential restriction modifier
Neonatal hepatosplenomegaly Is a Neonatal gastrointestinal disorder false Inferred relationship Existential restriction modifier
Neonatal hepatosplenomegaly Occurrence Neonatal true Inferred relationship Existential restriction modifier 1
Neonatal hepatosplenomegaly Finding site Splenic structure false Inferred relationship Existential restriction modifier
Neonatal hepatosplenomegaly Finding site Liver structure false Inferred relationship Existential restriction modifier 2
Neonatal hepatosplenomegaly Associated morphology Hypertrophy false Inferred relationship Existential restriction modifier 2
Neonatal hepatosplenomegaly Finding site Gastrointestinal tract structure false Inferred relationship Existential restriction modifier
Neonatal hepatosplenomegaly Is a Perinatal disorders of liver and/or biliary system false Inferred relationship Existential restriction modifier
Neonatal hepatosplenomegaly Is a Disorder of hematopoietic system in newborn true Inferred relationship Existential restriction modifier
Neonatal hepatosplenomegaly Associated morphology Hypertrophy false Inferred relationship Existential restriction modifier 1
Neonatal hepatosplenomegaly Finding site Splenic structure false Inferred relationship Existential restriction modifier 1
Neonatal hepatosplenomegaly Associated morphology Enlargement true Inferred relationship Existential restriction modifier 2
Neonatal hepatosplenomegaly Finding site Liver structure false Inferred relationship Existential restriction modifier 2
Neonatal hepatosplenomegaly Associated morphology Enlargement true Inferred relationship Existential restriction modifier 1
Neonatal hepatosplenomegaly Finding site Splenic structure false Inferred relationship Existential restriction modifier 1
Neonatal hepatosplenomegaly Associated morphology Enlargement false Inferred relationship Existential restriction modifier 3
Neonatal hepatosplenomegaly Associated morphology Enlargement false Inferred relationship Existential restriction modifier 4
Neonatal hepatosplenomegaly Finding site Entire liver false Inferred relationship Existential restriction modifier 4
Neonatal hepatosplenomegaly Finding site Entire spleen false Inferred relationship Existential restriction modifier 3
Neonatal hepatosplenomegaly Is a Disorder of digestive system specific to fetus OR newborn true Inferred relationship Existential restriction modifier
Neonatal hepatosplenomegaly Finding site Entire liver true Inferred relationship Existential restriction modifier 1
Neonatal hepatosplenomegaly Finding site Entire spleen true Inferred relationship Existential restriction modifier 2
Neonatal hepatosplenomegaly Occurrence Neonatal true Inferred relationship Existential restriction modifier 2

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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