idiopathic congenital hypothyroidism
Go to external page http://purl.obolibrary.org/obo/MONDO_0019858
Idiopathic congenital hypothyroidism is a type of primary congenital hypothyroidism whose cause and prevalence are unknown. [ Orphanet:95717 ]
This is just here as a test because I lose it
Term information
database
cross reference
- SCTID:717334008 (MONDO:equivalentTo)
- Orphanet:95717 (MONDO:equivalentTo)
- MEDGEN:901252 (MONDO:equivalentTo)
- UMLS:C4273913 (MONDO:equivalentTo)
- GARD:19298 (MONDO:GARD)
Subsets
ordo_disorder, gard_rare, rare, nord_rare, orphanet_rare
exactMatch
http://www.orpha.net/ORDO/Orphanet_95717
http://identifiers.org/snomedct/717334008
http://linkedlifedata.com/resource/umls/id/C4273913
http://identifiers.org/medgen/901252