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80473005: Neonatal hyperhistidinemia (disorder)


Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
133535014 Neonatal hyperhistidinemia en Synonym Active Case insensitive SNOMED CT core
504435014 Neonatal hyperhistidinaemia en Synonym Active Case insensitive SNOMED CT core
821637019 Neonatal hyperhistidinemia (disorder) en Fully specified name Active Case insensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Neonatal hyperhistidinaemia Finding site Body system structure false Inferred relationship Some
Neonatal hyperhistidinaemia Is a Neonatal disorder false Inferred relationship Some
Neonatal hyperhistidinaemia Occurrence Neonatal true Inferred relationship Some 1
Neonatal hyperhistidinaemia Is a Endocrine AND/OR metabolic disorder specific to the fetus OR newborn false Inferred relationship Some
Neonatal hyperhistidinaemia Is a Hereditary disorder of endocrine system false Inferred relationship Some
Neonatal hyperhistidinaemia Is a Congenital anomaly of endocrine gland false Inferred relationship Some
Neonatal hyperhistidinaemia Is a Disorder of histidine metabolism true Inferred relationship Some
Neonatal hyperhistidinaemia Is a Reproductive system hereditary disorder false Inferred relationship Some
Neonatal hyperhistidinaemia Is a Neonatal metabolic disorder true Inferred relationship Some
Neonatal hyperhistidinaemia Finding site Entire endocrine gonad false Inferred relationship Some
Neonatal hyperhistidinaemia Occurrence Neonatal false Inferred relationship Some
Neonatal hyperhistidinaemia Occurrence Congenital false Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

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