SNOMED CT

Last uploaded: August 28, 2024
Preferred Name

Congenital macroglossia
Synonyms

Congenital macroglossia (disorder)

Congenital hypertrophy of tongue

ID

http://purl.bioontology.org/ontology/SNOMEDCT/270516002

Active

1

altLabel

Congenital macroglossia (disorder)

Congenital hypertrophy of tongue

CASE SIGNIFICANCE ID

900000000000020002

900000000000448009

CTV3ID

XE2Qr

cui

C0009677

DEFINITION STATUS ID

900000000000073002

Effective time

20130131

Has associated morphology

http://purl.bioontology.org/ontology/SNOMEDCT/442021009

Has finding site

http://purl.bioontology.org/ontology/SNOMEDCT/181226008

Has pathological process

http://purl.bioontology.org/ontology/SNOMEDCT/308490002

INACTIVATION INDICATOR

900000000000482003

900000000000495008

notation

270516002

Occurs in

http://purl.bioontology.org/ontology/SNOMEDCT/255399007

prefLabel

Congenital macroglossia

Subset member

900000000000497000~MAPTARGET~XE2Qr

447562003~MAPRULE~TRUE

6011000124106~MAPADVICE~IF BECKWITH-WIEDEMANN SYNDROME CHOOSE Q87.3 | CONSIDER ADDITIONAL CODE TO IDENTIFY SPECIFIC CONDITION OR DISEASE | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

447562003~MAPTARGET~Q38.2

6011000124106~MAPGROUP~1

447562003~MAPADVICE~ALWAYS Q38.2

900000000000527005~TARGETCOMPONENT~52106009

900000000000490003~VALUEID~900000000000495008

900000000000508004~ACCEPTABILITYID~900000000000549004

447562003~MAPGROUP~1

6011000124106~MAPADVICE~ALWAYS Q38.2

900000000000489007~VALUEID~900000000000482003

447562003~CORRELATIONID~447561005

6011000124106~MAPCATEGORYID~447637006

900000000000509007~ACCEPTABILITYID~900000000000548007

900000000000508004~ACCEPTABILITYID~900000000000548007

6011000124106~MAPTARGET~Q87.3

447562003~MAPPRIORITY~1

6011000124106~MAPRULE~IFA 81780002 | Beckwith-Wiedemann syndrome (disorder) |

447562003~MAPCATEGORYID~447637006

6011000124106~MAPRULE~OTHERWISE TRUE

6011000124106~MAPCATEGORYID~447639009

6011000124106~MAPPRIORITY~1

6011000124106~CORRELATIONID~447561005

6011000124106~MAPTARGET~Q38.2

900000000000509007~ACCEPTABILITYID~900000000000549004

6011000124106~MAPPRIORITY~2

6011000124106~MAPRULE~IFA 81780002 | Beckwith-Wiedemann syndrome |

tui

T019

Type ID

900000000000003001

900000000000013009

subClassOf

http://purl.bioontology.org/ontology/SNOMEDCT/60447007

http://purl.bioontology.org/ontology/SNOMEDCT/25273001

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Mapping To Ontology Source
http://purl.bioontology.org/ontology/ICD10CM/Q38.2 ICD10CM CUI
http://purl.bioontology.org/ontology/RCD/XE2Qr RCD CUI
http://purl.bioontology.org/ontology/MDRFRE/10025391 MDRFRE CUI
http://purl.bioontology.org/ontology/MDRGER/10025391 MDRGER CUI
http://purl.bioontology.org/ontology/MEDDRA/10025391 MEDDRA CUI
http://purl.bioontology.org/ontology/MESH/C531735 MESH CUI
http://purl.bioontology.org/ontology/MDRGER/10063437 MDRGER CUI
http://purl.bioontology.org/ontology/ICD9CM/750.15 ICD9CM CUI
http://purl.bioontology.org/ontology/MDRFRE/10063437 MDRFRE CUI
http://purl.bioontology.org/ontology/MEDDRA/10063437 MEDDRA CUI
http://purl.bioontology.org/ontology/SNMI/D4-52011 SNMI CUI
http://purl.bioontology.org/ontology/SCTSPA/270516002 SCTSPA CUI
http://purl.bioontology.org/ontology/ICD10/Q38.2 ICD10 CUI
http://purl.obolibrary.org/obo/MONDO_0007927 MONDO LOOM
http://www.limics.org/hrdo/rdfns#pat_id_535 HRDO LOOM
http://www.orpha.net/ORDO/Orphanet_2430 ORDO LOOM
http://phenomebrowser.net/ontologies/mesh/mesh.owl#C531735 RH-MESH LOOM
rgo:24231 GAMUTS LOOM
http://purl.bioontology.org/ontology/RCD/XE2Qr RCD LOOM
http://sbmi.uth.tmc.edu/ontology/ochv#3273 OCHV LOOM
http://purl.bioontology.org/ontology/MESH/C531735 MESH LOOM
http://www.semanticweb.org/ontologies/2012/5/Ontology1338526551855.owl#Congenital_macroglossia RPO LOOM
http://purl.bioontology.org/ontology/MEDDRA/10063437 MEDDRA LOOM
http://purl.obolibrary.org/obo/MONDO_0007927 CCONT LOOM
http://purl.obolibrary.org/obo/MONDO_0007927 EFO LOOM
http://purl.obolibrary.org/obo/MONDO_0007927 DOVES LOOM