A thyroid hormone deficiency present from birth. [ Orphanet:442 ]
Synonyms: congenital iodine deficiency syndrome congenital hypothyroidism
Term information
- SCTID:217710005 (MONDO:equivalentTo)
- SCTID:190268003 (MONDO:equivalentTo)
- DOID:0050328 (MONDO:equivalentTo)
- icd11.foundation:602450215 (Orphanet:442)
- MedDRA:10010510 (Orphanet:442/e)
- MEDGEN:41344 (MONDO:equivalentTo)
- ICD9:269.3
- NCIT:C26734 (MONDO:equivalentTo)
- ICD9:243 (DOID:0050328)
- UMLS:C0010308 (MONDO:equivalentTo)
- NANDO:2200333 (https://orcid.org/0000-0003-0011-764X)
- MESH:D003409 (Orphanet:442/e)
- ICD9:759.89
- GARD:1487 (MONDO:GARD)
- Orphanet:442 (MONDO:equivalentTo)
gard_rare, otar, disease_grouping, rare, nord_rare, ordo_group_of_disorders
http://purl.obolibrary.org/obo/DOID_0050328
http://www.orpha.net/ORDO/Orphanet_442
http://identifiers.org/snomedct/190268003
http://linkedlifedata.com/resource/umls/id/C0010308
http://identifiers.org/medgen/41344
http://purl.obolibrary.org/obo/NCIT_C26734
http://identifiers.org/snomedct/217710005
http://identifiers.org/mesh/D003409
infantile hypothyroidism
fetal iodine deficiency syndrome
congenital hypothyroidism not due to iodine deficiency
congenital goitre
congenital goiter
foetal iodine deficiency syndrome
cretinism