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425522009: Hyperammonemic encephalopathy (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2007. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
2662616017 Hyperammonemic encephalopathy (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
2674242012 Hyperammonemic encephalopathy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
1822911000195114 encefalopatia iperammonemica it Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5295781000241111 encéphalopathie hyperammoniémique fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


1 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Hyperammonemic encephalopathy (disorder) Is a Toxic encephalopathy true Inferred relationship Some
Hyperammonemic encephalopathy (disorder) Associated with Hyperammonemia true Inferred relationship Some 1
Hyperammonemic encephalopathy (disorder) Finding site Brain tissue structure false Inferred relationship Some 2
Hyperammonemic encephalopathy (disorder) Finding site Brain structure false Inferred relationship Some
Hyperammonemic encephalopathy (disorder) Is a Central nervous system complication true Inferred relationship Some
Hyperammonemic encephalopathy (disorder) Finding site Brain structure true Inferred relationship Some 2

Inbound Relationships Type Active Source Characteristic Refinability Group
A rare, hereditary inborn error of metabolism characterized by an acute onset of encephalopathy in infancy or early childhood. Apart from these episodic acute events, the disorder shows a relatively benign course. Multiple metabolic abnormalities are present, including metabolic acidosis, respiratory alkalosis, hypoglycemia, increased serum lactate and alanine. Is a True Hyperammonemic encephalopathy (disorder) Inferred relationship Some

This concept is not in any reference sets

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