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transient congenital hypothyroidism

Go to external page http://purl.obolibrary.org/obo/MONDO_0015792

A common, self-limiting thyroid disorder seen in preterm infants that is characterized by abnormally low serum levels of thyroxine and free thyroxine with normal serum levels of thyroid stimulating hormone. [ NCIT:C113171 ]

Synonyms: THOP hypothyroxinemia of prematurity transient hypothyroxinemia of prematurity

This is just here as a test because I lose it

Term information

database cross reference
  • UMLS:C3827793 (MONDO:equivalentTo)
  • GARD:20142 (MONDO:GARD)
  • icd11.foundation:592246939 (Orphanet:178045)
  • NCIT:C113171 (MONDO:equivalentTo)
  • Orphanet:178045 (MONDO:equivalentTo)
  • MEDGEN:820541 (MONDO:equivalentTo)
  • SCTID:119181000119104 (MONDO:equivalentTo)
Subsets

gard_rare, disease_grouping, rare, nord_rare, ordo_group_of_disorders

exactMatch

http://purl.obolibrary.org/obo/NCIT_C113171

http://identifiers.org/snomedct/119181000119104

http://www.orpha.net/ORDO/Orphanet_178045

http://identifiers.org/medgen/820541

http://linkedlifedata.com/resource/umls/id/C3827793

id

MONDO:0015792

Term relations