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congenital hypothyroidism

Go to external page http://purl.obolibrary.org/obo/MONDO_0018612

A thyroid hormone deficiency present from birth. [ Orphanet:442 ]

Synonyms: congenital iodine deficiency syndrome congenital hypothyroidism

This is just here as a test because I lose it

Term information

database cross reference
  • SCTID:190268003 (MONDO:equivalentTo)
  • MedDRA:10010510 (Orphanet:442/e)
  • SCTID:217710005 (MONDO:equivalentTo)
  • Orphanet:442 (MONDO:equivalentTo)
  • MESH:D003409 (Orphanet:442/e)
  • UMLS:C0010308 (Orphanet:442/e)
  • DOID:0050328 (MONDO:equivalentTo)
  • GARD:1487 (Orphanet:442)
  • ICD9:759.89
  • ICD9:269.3
  • NCIT:C26734 (MONDO:equivalentTo)
  • ICD9:243 (DOID:0050328)
Subsets

gard_rare, disease_grouping, rare, nord_rare, orphanet_rare, ordo_group_of_disorders

IAO 0000233

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

closeMatch

http://identifiers.org/meddra/10010510

exactMatch

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

http://identifiers.org/snomedct/190268003

http://www.orpha.net/ORDO/Orphanet_442

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

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

http://identifiers.org/snomedct/217710005

http://identifiers.org/mesh/D003409

has related synonym

infantile hypothyroidism

fetal iodine deficiency syndrome

congenital hypothyroidism not due to iodine deficiency

congenital goitre

congenital goiter

foetal iodine deficiency syndrome

cretinism

id

MONDO:0018612

Term relations

Subclass of: