SNOMED CT

Last uploaded: January 31, 2024
Preferred Name

Hyperphenylalaninemia

Synonyms

Hyperphenylalaninemia (disorder)

Hyperphenylalaninaemia

ID

http://purl.bioontology.org/ontology/SNOMEDCT/68528007

Active

1

altLabel

Hyperphenylalaninemia (disorder)

Hyperphenylalaninaemia

CASE SIGNIFICANCE ID

900000000000020002

900000000000448009

CTV3ID

XUIyE

cui

C0751435

DEFINITION STATUS ID

900000000000074008

Effective time

20020131

notation

68528007

prefLabel

Hyperphenylalaninemia

Subset member

447562003~MAPADVICE~IF CLASSICAL PHENYLKETONURIA CHOOSE E70.0 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

447562003~MAPRULE~TRUE

6011000124106~MAPRULE~IFA 7573000 | Classical phenylketonuria (disorder) |

6011000124106~MAPTARGET~E70.1

447562003~MAPTARGET~E70.1

6011000124106~MAPADVICE~ALWAYS E70.1 | DESCENDANTS NOT EXHAUSTIVELY MAPPED

6011000124106~MAPADVICE~MAP SOURCE CONCEPT CANNOT BE CLASSIFIED WITH AVAILABLE DATA

6011000124106~MAPTARGET~

6011000124106~MAPCATEGORYID~447638001

447562003~MAPTARGET~E70.2

6011000124106~MAPADVICE~IF PERSISTENT HYPERPHENYLALANINEMIA AND TYROSINEMIA CHOOSE E70.21 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

6011000124106~MAPGROUP~1

6011000124106~MAPGROUP~2

447562003~MAPADVICE~ALWAYS E70.1

447562003~MAPGROUP~2

447562003~MAPRULE~IFA 40751003 | Persistent hyperphenylalaninemia AND tyrosinemia (disorder) |

447562003~MAPADVICE~MAP SOURCE CONCEPT CANNOT BE CLASSIFIED WITH AVAILABLE DATA

900000000000508004~ACCEPTABILITYID~900000000000549004

447562003~MAPGROUP~1

447562003~CORRELATIONID~447561005

447562003~MAPRULE~OTHERWISE TRUE

447562003~MAPRULE~IFA 7573000 | Classical phenylketonuria (disorder) |

6011000124106~MAPCATEGORYID~447637006

900000000000509007~ACCEPTABILITYID~900000000000548007

6011000124106~MAPRULE~IFA 40751003 | Persistent hyperphenylalaninemia AND tyrosinemia (disorder) |

900000000000508004~ACCEPTABILITYID~900000000000548007

447562003~MAPTARGET~

447562003~MAPPRIORITY~1

6011000124106~MAPADVICE~IF CLASSICAL PHENYLKETONURIA CHOOSE E70.0 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

447562003~MAPCATEGORYID~447637006

6011000124106~MAPRULE~OTHERWISE TRUE

447562003~MAPTARGET~E70.0

900000000000497000~MAPTARGET~XUIyE

447562003~MAPADVICE~IF PERSISTENT HYPERPHENYLALANINEMIA CHOOSE E70.1 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

6011000124106~MAPCATEGORYID~447639009

447562003~MAPPRIORITY~3

447562003~MAPCATEGORYID~447639009

6011000124106~MAPPRIORITY~1

6011000124106~CORRELATIONID~447561005

447562003~MAPPRIORITY~2

6011000124106~MAPADVICE~ALWAYS E70.1

6011000124106~MAPRULE~TRUE

6011000124106~MAPTARGET~E70.21

447562003~MAPRULE~IFA 440009 | Persistent hyperphenylalaninemia (disorder) |

900000000000509007~ACCEPTABILITYID~900000000000549004

6011000124106~MAPPRIORITY~2

6011000124106~MAPTARGET~E70.0

447562003~MAPCATEGORYID~447638001

447562003~MAPADVICE~IF PERSISTENT HYPERPHENYLALANINEMIA AND TYROSINEMIA CHOOSE E70.2 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

tui

T047

Type ID

900000000000003001

900000000000013009

subClassOf

http://purl.bioontology.org/ontology/SNOMEDCT/12957008

http://purl.bioontology.org/ontology/SNOMEDCT/46556004

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Delete Mapping To Ontology Source
http://purl.bioontology.org/ontology/CSP/1849-1177 CRISP CUI
http://purl.bioontology.org/ontology/MDRFRE/10084106 MDRFRE CUI
http://purl.bioontology.org/ontology/LNC/LA21167-4 LOINC CUI
http://purl.bioontology.org/ontology/MEDDRA/10084114 MEDDRA CUI
http://purl.bioontology.org/ontology/MEDDRA/10084106 MEDDRA CUI
http://purl.bioontology.org/ontology/SCTSPA/68528007 SCTSPA CUI
http://purl.bioontology.org/ontology/MDRFRE/10084114 MDRFRE CUI
http://purl.bioontology.org/ontology/MSHFRE/D010661 MSHFRE CUI
http://purl.bioontology.org/ontology/OMIM/MTHU010142 OMIM CUI
http://purl.bioontology.org/ontology/MDRGER/10084106 MDRGER CUI
http://purl.bioontology.org/ontology/SNMI/D6-A1110 SNMI CUI
http://purl.bioontology.org/ontology/MDRGER/10084114 MDRGER CUI
http://purl.bioontology.org/ontology/MESH/D010661 MESH CUI
http://purl.obolibrary.org/obo/HP_0004923 HP LOOM
http://purl.obolibrary.org/obo/HP_0004923 HP LOOM
http://www.orpha.net/ORDO/Orphanet_238583 EFO LOOM
http://purl.obolibrary.org/obo/HP_0004923 OBA LOOM
http://purl.bioontology.org/ontology/CSP/1849-1177 CRISP LOOM
http://onstr.googlecode.com/svn/tags/currentRelease/2014-09-03/ONSTR.owl#ONSTR_7546388 ONSTR LOOM
http://purl.bioontology.org/ontology/LNC/LA21167-4 LOINC LOOM
http://purl.bioontology.org/ontology/MEDDRA/10084114 MEDDRA LOOM
http://www.phoc.org.cn/pmo/class/PMO_00003768 PMAPP-PMO LOOM
http://sbmi.uth.tmc.edu/ontology/ochv#C0751435 OCHV LOOM
http://www.limics.org/hrdo/rdfns#pat_id_19279 HRDO LOOM
http://purl.bioontology.org/ontology/OMIM/MTHU010142 OMIM LOOM
http://identifiers.org/omim/261600 REXO LOOM
http://identifiers.org/omim/261600 GEXO LOOM
http://identifiers.org/omim/261600 RETO LOOM
http://www.gamuts.net/entity#hyperphenylalaninemia GAMUTS LOOM
http://purl.obolibrary.org/obo/HP_0004923 UPHENO LOOM
http://purl.obolibrary.org/obo/HP_0004923 MAXO LOOM
http://purl.obolibrary.org/obo/OMIM_261600 CCO LOOM
http://purl.jp/bio/4/id/200906086179712502 IOBC LOOM
http://www.gamuts.net/entity#hyperphenylalaninemia GAMUTS REST