SNOMED CT

Last uploaded: January 31, 2024
Preferred Name

Congenital hypothyroidism

Synonyms

Congenital hypothyroidism (disorder)

ID

http://purl.bioontology.org/ontology/SNOMEDCT/190268003

Active

1

altLabel

Congenital hypothyroidism (disorder)

Associated finding of

http://purl.bioontology.org/ontology/SNOMEDCT/428300000

CASE SIGNIFICANCE ID

900000000000448009

Cause of

http://purl.bioontology.org/ontology/SNOMEDCT/206457007

CTV3ID

C03..

cui

C0010308

DEFINITION STATUS ID

900000000000073002

Effective time

20140731

Focus of

http://purl.bioontology.org/ontology/SNOMEDCT/400984005

Has finding site

http://purl.bioontology.org/ontology/SNOMEDCT/69748006

notation

190268003

Occurs in

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

prefLabel

Congenital hypothyroidism

Subset member

447562003~MAPRULE~TRUE

447562003~MAPTARGET~Q89.2

6011000124106~MAPGROUP~1

6011000124106~MAPADVICE~ALWAYS E03.1 | DESCENDANTS NOT EXHAUSTIVELY MAPPED

447562003~MAPTARGET~E03.1

447562003~MAPGROUP~1

447562003~CORRELATIONID~447561005

447562003~MAPRULE~OTHERWISE TRUE

6011000124106~MAPCATEGORYID~447637006

900000000000509007~ACCEPTABILITYID~900000000000548007

447562003~MAPRULE~IFA 93359004 | Congenital malposition of the thyroid gland (disorder) |

900000000000508004~ACCEPTABILITYID~900000000000548007

447562003~MAPRULE~IFA 84781002 | Sporadic cretinism (disorder) |

447562003~MAPTARGET~E00.9

900000000000497000~MAPTARGET~C03..

447562003~MAPADVICE~ALWAYS E03.1

447562003~MAPPRIORITY~1

447562003~MAPCATEGORYID~447637006

447562003~MAPTARGET~E03.0

447562003~MAPPRIORITY~3

447562003~MAPADVICE~IF SPORADIC CRETINISM CHOOSE E00.9 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

447562003~MAPADVICE~IF CONGENITAL HYPOTHYROIDISM WITH DIFFUSE GOITER CHOOSE E03.0 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

447562003~MAPCATEGORYID~447639009

6011000124106~MAPTARGET~E03.1

6011000124106~MAPPRIORITY~1

447562003~MAPRULE~IFA 278503003 | Congenital hypothyroidism with diffuse goiter (disorder) |

6011000124106~CORRELATIONID~447561005

447562003~MAPADVICE~IF CONGENITAL MALPOSITION OF THE THYROID GLAND CHOOSE Q89.2 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

447562003~MAPPRIORITY~2

6011000124106~MAPRULE~TRUE

447562003~MAPPRIORITY~4

tui

T047

Type ID

900000000000003001

900000000000013009

subClassOf

http://purl.bioontology.org/ontology/SNOMEDCT/66091009

http://purl.bioontology.org/ontology/SNOMEDCT/40930008

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Create mapping

Delete Mapping To Ontology Source
http://purl.bioontology.org/ontology/LNC/LP56766-6 LOINC CUI
http://purl.bioontology.org/ontology/SCTSPA/190268003 SCTSPA CUI
http://purl.bioontology.org/ontology/RCD/C03.. RCD CUI
http://purl.bioontology.org/ontology/MEDDRA/10021115 MEDDRA CUI
http://purl.bioontology.org/ontology/MEDDRA/10010510 MEDDRA CUI
http://purl.bioontology.org/ontology/LNC/MTHU025182 LOINC CUI
http://purl.bioontology.org/ontology/OMIM/MTHU003987 OMIM CUI
http://purl.bioontology.org/ontology/MDRFRE/10011381 MDRFRE CUI
http://purl.bioontology.org/ontology/ICPC2P/T80007 ICPC2P CUI
http://purl.bioontology.org/ontology/NDFRT/N0000171688 NDFRT CUI
http://purl.bioontology.org/ontology/MDRGER/10010510 MDRGER CUI
http://purl.bioontology.org/ontology/ICD9CM/243 ICD9CM CUI
http://purl.bioontology.org/ontology/MDRFRE/10021115 MDRFRE CUI
http://purl.bioontology.org/ontology/WHOFRE/0800 WHOFRE CUI
http://purl.bioontology.org/ontology/MDRFRE/10010510 MDRFRE CUI
http://purl.bioontology.org/ontology/MDRGER/10011381 MDRGER CUI
http://purl.bioontology.org/ontology/SNMI/D4-01830 SNMI CUI
http://purl.bioontology.org/ontology/ICPC2P/T86004 ICPC2P CUI
http://purl.bioontology.org/ontology/ICD10CM/E03.1 ICD10CM CUI
http://purl.bioontology.org/ontology/MEDDRA/10011381 MEDDRA CUI
http://purl.bioontology.org/ontology/MSHFRE/D003409 MSHFRE CUI
http://purl.bioontology.org/ontology/CSP/2928-6883 CRISP CUI
http://purl.bioontology.org/ontology/MDRGER/10021115 MDRGER CUI
http://purl.bioontology.org/ontology/CST/CRETIN COSTART CUI
http://purl.bioontology.org/ontology/WHO/0800 WHO-ART CUI
http://purl.bioontology.org/ontology/OMIM/MTHU038801 OMIM CUI
http://purl.bioontology.org/ontology/MESH/D003409 MESH CUI
http://purl.obolibrary.org/obo/DOID_0050328 DOID LOOM
http://purl.obolibrary.org/obo/MONDO_0018612 EFO LOOM
http://purl.obolibrary.org/obo/DOID_0050328 DOID LOOM
http://purl.obolibrary.org/obo/MONDO_0018612 MONDO LOOM
http://purl.obolibrary.org/obo/HP_0000851 HP LOOM
http://phenomebrowser.net/ontologies/mesh/mesh.owl#D003409 RH-MESH LOOM
http://purl.bioontology.org/ontology/LNC/LP56766-6 LOINC LOOM
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#Congenital_Hypothyroidism CSEO LOOM
http://purl.obolibrary.org/obo/MONDO_0018612 DOVES LOOM
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C26734 NCIT LOOM
http://purl.bioontology.org/ontology/RCTV2/C03..00 RCTV2 LOOM
http://purl.bioontology.org/ontology/RCD/C03.. RCD LOOM
http://purl.bioontology.org/ontology/MEDDRA/10010510 MEDDRA LOOM
http://purl.obolibrary.org/obo/OMIT_0004704 OMIT LOOM
http://phenomebrowser.net/ontologies/mesh/mesh.owl#C19.297.155 RH-MESH LOOM
http://phenomebrowser.net/ontologies/mesh/mesh.owl#C05.116.132.256 RH-MESH LOOM
http://purl.obolibrary.org/obo/HP_0000851 UPHENO LOOM
http://purl.bioontology.org/ontology/LNC/MTHU025182 LOINC LOOM
http://www.gamuts.net/entity#congenital_hypothyroidism GAMUTS LOOM
http://purl.bioontology.org/ontology/OMIM/MTHU003987 OMIM LOOM
http://phenomebrowser.net/ontologies/mesh/mesh.owl#C16.320.240.625 RH-MESH LOOM
http://phenomebrowser.net/ontologies/mesh/mesh.owl#C05.116.099.343.347 RH-MESH LOOM
http://sbmi.uth.tmc.edu/ontology/ochv#C0221001 OCHV LOOM
http://purl.bioontology.org/ontology/ICD9CM/243 ICD9CM LOOM
http://www.phoc.org.cn/pmo/class/PMO_00037004 PMAPP-PMO LOOM
http://phenomebrowser.net/ontologies/mesh/mesh.owl#C19.874.482.281 RH-MESH LOOM
http://www.orpha.net/ORDO/Orphanet_442 ORDO LOOM
http://sbmi.uth.tmc.edu/ontology/ochv#C0342200 OCHV LOOM
http://purl.bioontology.org/ontology/ICPC2P/T86004 ICPC2P LOOM
http://purl.obolibrary.org/obo/DOID_0050328 DTO LOOM
http://purl.obolibrary.org/obo/DOID_0050328 BAO LOOM
http://purl.obolibrary.org/obo/DOID_0050328 HHEAR LOOM
http://purl.obolibrary.org/obo/DOID_0050328 NIFSTD LOOM
http://purl.obolibrary.org/obo/DOID_0050328 MIDO LOOM
http://purl.obolibrary.org/obo/DOID_0050328 FNS-H LOOM
http://purl.obolibrary.org/obo/NCIT_C26734 BERO LOOM
http://www.limics.org/hrdo/rdfns#pat_id_760 HRDO LOOM
http://purl.bioontology.org/ontology/MESH/D003409 MESH LOOM
http://www.owl-ontologies.com/Ontology1358660052.owl#Congenital_Hypothyroidism PEDTERM LOOM
http://www.gamuts.net/entity#congenital_hypothyroidism GAMUTS REST