loading...| Preferred Name |
Hyperammonemia |
|
| Synonyms |
Hyperammonaemia Hyperammonemia (disorder) |
|
| ID |
http://purl.bioontology.org/ontology/SNOMEDCT/9360008 |
|
| Active |
1 |
|
| altLabel |
Hyperammonaemia Hyperammonemia (disorder) |
|
| Associated with | ||
| CASE SIGNIFICANCE ID |
900000000000020002 900000000000448009 |
|
| Cause of | ||
| CTV3ID |
XUO1y |
|
| cui |
C0220994 |
|
| DEFINITION STATUS ID |
900000000000074008 |
|
| Effective time |
20020131 |
|
| notation |
9360008 |
|
| prefLabel |
Hyperammonemia |
|
| Subset member |
6011000124106~MAPTARGET~E72.4 447562003~MAPRULE~TRUE 900000000000497000~MAPTARGET~XUO1y 447562003~MAPTARGET~E72.2 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 | |
|
| tui |
T047 |
|
| Type ID |
900000000000003001 900000000000013009 |
|
| subClassOf |