SNOMED CT

Last uploaded: January 16, 2025
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Id http://purl.bioontology.org/ontology/SNOMEDCT/9360008
http://purl.bioontology.org/ontology/SNOMEDCT/9360008
Preferred Name

Hyperammonemia
Synonyms
Hyperammonaemia
Hyperammonemia (disorder)
Type http://www.w3.org/2002/07/owl#Class

All Properties

altLabel
Hyperammonaemia
Hyperammonemia (disorder)
prefLabel
Hyperammonemia
Associated with
Type ID
900000000000003001
900000000000013009
CASE SIGNIFICANCE ID
900000000000020002
900000000000448009
notation
9360008
Effective time
20020131
Active
1
subClassOf
Semantic type UMLS property
Cause of
type
Subset member
6011000124106~MAPTARGET~E72.4
447562003~MAPRULE~TRUE
900000000000497000~MAPTARGET~XUO1y
447562003~MAPTARGET~E72.2
6011000124106~MAPADVICE~IF HYPERINSULINISM AND HYPERAMMONEMIA SYNDROME CHOOSE E16.1 | CONSIDER ADDITIONAL CODE TO IDENTIFY SPECIFIC CONDITION OR DISEASE | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT
6011000124106~MAPADVICE~IF CONGENITAL HYPERAMMONEMIA, TYPE I CHOOSE E72.29 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT
6011000124106~MAPPRIORITY~4
6011000124106~MAPRULE~IFA 57119000 | Hyperammonemia, type III (disorder) |
6011000124106~MAPADVICE~MAP SOURCE CONCEPT CANNOT BE CLASSIFIED WITH AVAILABLE DATA
6011000124106~MAPRULE~IFA 62522004 | Congenital hyperammonemia, type I |
6011000124106~MAPADVICE~IF ORNITHINE CARBAMOYLTRANSFERASE DEFICIENCY CHOOSE E72.4 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT
6011000124106~MAPTARGET~
6011000124106~MAPCATEGORYID~447638001
6011000124106~MAPGROUP~1
6011000124106~MAPGROUP~2
6011000124106~MAPADVICE~IF HYPERAMMONEMIA, TYPE III CHOOSE E72.29 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT
6011000124106~MAPRULE~IFA 30287008 | Hyperornithinemia-hyperammonemia-homocitrullinuria syndrome (disorder) |
6011000124106~MAPADVICE~IF TRANSIENT HYPERAMMONEMIA IN INFANCY CHOOSE P74.6 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT
6011000124106~MAPRULE~IFA 11225002 | Transient hyperammonemia in infancy (disorder) |
6011000124106~MAPTARGET~P74.6
900000000000508004~ACCEPTABILITYID~900000000000549004
447562003~MAPGROUP~1
6011000124106~MAPADVICE~ALWAYS E72.20
6011000124106~MAPRULE~IFA 718106009 | Hyperinsulinism and hyperammonemia syndrome |
447562003~CORRELATIONID~447561005
6011000124106~MAPRULE~IFA 57119000 | Hyperammonemia, type III |
6011000124106~MAPCATEGORYID~447637006
900000000000509007~ACCEPTABILITYID~900000000000548007
6011000124106~MAPRULE~IFA 62522004 | Congenital hyperammonemia, type I (disorder) |
900000000000508004~ACCEPTABILITYID~900000000000548007
6011000124106~MAPTARGET~E72.29
6011000124106~MAPRULE~IFA 718106009 | Hyperinsulinism and hyperammonemia syndrome (disorder) |
6011000124106~MAPADVICE~IF HYPERORNITHINEMIA-HYPERAMMONEMIA-HOMOCITRULLINURIA SYNDROME CHOOSE E72.4 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT
6011000124106~MAPADVICE~IF HYPERINSULINISM AND HYPERAMMONEMIA SYNDROME CHOOSE E16.1 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT
447562003~MAPPRIORITY~1
447562003~MAPCATEGORYID~447637006
6011000124106~MAPRULE~IFA 11225002 | Transient hyperammonemia in infancy |
6011000124106~MAPTARGET~E16.1
6011000124106~MAPRULE~OTHERWISE TRUE
6011000124106~MAPPRIORITY~5
6011000124106~MAPRULE~IFA 80908008 | Ornithine carbamoyltransferase deficiency |
6011000124106~MAPRULE~IFA 80908008 | Ornithine carbamoyltransferase deficiency (disorder) |
6011000124106~MAPCATEGORYID~447639009
447562003~MAPADVICE~ALWAYS E72.2
6011000124106~MAPPRIORITY~1
6011000124106~MAPPRIORITY~6
6011000124106~MAPADVICE~IF HYPERINSULINISM AND HYPERAMMONEMIA SYNDROME CHOOSE E72.20 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT
6011000124106~CORRELATIONID~447561005
6011000124106~MAPTARGET~E72.20
6011000124106~MAPPRIORITY~3
900000000000509007~ACCEPTABILITYID~900000000000549004
6011000124106~MAPPRIORITY~2
6011000124106~MAPRULE~IFA 30287008 | Hyperornithinemia-hyperammonemia-homocitrullinuria syndrome |
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DEFINITION STATUS ID
900000000000074008
tui
T047
CTV3ID
XUO1y
cui
C0220994
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