Cell Culture Ontology

Last uploaded: July 23, 2014
Preferred Name

congenital hypothyroidism
Synonyms

congenital hypothyroidism not due to iodine deficiency

congenital goitre

foetal iodine deficiency syndrome

congenital goiter

fetal iodine deficiency syndrome

infantile hypothyroidism

cretinism

congenital iodine deficiency syndrome

congenital hypothyroidism

Definitions

A thyroid hormone deficiency present from birth.

ID

http://purl.obolibrary.org/obo/MONDO_0018612

database_cross_reference

ICD9:759.89

SCTID:217710005

MESH:D003409

NANDO:2200333

MEDGEN:41344

NCIT:C26734

MedDRA:10010510

SCTID:190268003

icd11.foundation:602450215

Orphanet:442

UMLS:C0010308

DOID:0050328

GARD:1487

ICD9:243

ICD9:269.3

definition

A thyroid hormone deficiency present from birth.

has_exact_synonym

congenital iodine deficiency syndrome

congenital hypothyroidism

has_related_synonym

congenital hypothyroidism not due to iodine deficiency

congenital goitre

foetal iodine deficiency syndrome

congenital goiter

fetal iodine deficiency syndrome

infantile hypothyroidism

cretinism

IAO_0000233

https://github.com/monarch-initiative/mondo/issues/4069

id

MONDO:0018612

in_subset

http://purl.obolibrary.org/obo/mondo/mondo-base#rare

http://purl.obolibrary.org/obo/mondo/mondo-base#otar

http://purl.obolibrary.org/obo/mondo/mondo-base#gard_rare

http://purl.obolibrary.org/obo/mondo/mondo-base#ordo_group_of_disorders

http://purl.obolibrary.org/obo/mondo/mondo-base#disease_grouping

http://purl.obolibrary.org/obo/mondo/mondo-base#nord_rare

label

congenital hypothyroidism

notation

MONDO:0018612

preferred label

congenital hypothyroidism

prefLabel

congenital hypothyroidism

skos_closeMatch

http://identifiers.org/meddra/10010510

skos_exactMatch

http://identifiers.org/snomedct/190268003

http://identifiers.org/medgen/41344

http://identifiers.org/snomedct/217710005

http://identifiers.org/mesh/D003409

http://purl.obolibrary.org/obo/mondo/sources/icd11foundation/602450215

http://purl.obolibrary.org/obo/DOID_0050328

http://purl.obolibrary.org/obo/NCIT_C26734

http://linkedlifedata.com/resource/umls/id/C0010308

http://purl.obolibrary.org/obo/Orphanet_442

subClassOf

http://www.ebi.ac.uk/efo/EFO_0004705

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Delete Mapping To Ontology Source
http://purl.obolibrary.org/obo/MONDO_0018612 MONDO SAME_URI
http://purl.obolibrary.org/obo/MONDO_0018612 EFO SAME_URI
http://purl.obolibrary.org/obo/MONDO_0018612 DOVES SAME_URI
http://purl.obolibrary.org/obo/MONDO_0018612 MONDO 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 EFO 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 HP LOOM
http://purl.obolibrary.org/obo/HP_0000851 UPHENO LOOM
http://purl.bioontology.org/ontology/LNC/MTHU025182 LOINC LOOM
http://nanbyodata.jp/ontology/NANDO_2200333 NANDO 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/SNOMEDCT/190268003 SNOMEDCT 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 DOID 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 DDSS 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
rgo:29831 GAMUTS 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