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central congenital hypothyroidism

Go to external page http://purl.obolibrary.org/obo/MONDO_0016410

Central or secondary congenital hypothyroidism is a type of permanent congenital hypothyroidism characterized by permanent thyroid hormone deficiency that is present from birth and secondary to a disorder in the thyroid-stimulating hormone (TSH) - thyrotropin-releasing hormone (TRH) system. [ Orphanet:226298 ]

Synonyms: hypothalamic-pituitary hypothyroidism secondary hypothyroidism thyrotropin deficiency TSH deficiency central hypothyroidism thyroid stimulating hormone deficiency

This is just here as a test because I lose it

Term information

database cross reference
  • GARD:12280 (MONDO:GARD)
  • NANDO:2200332 (https://orcid.org/0000-0003-0011-764X)
  • NCIT:C113144 (MONDO:equivalentTo)
  • NANDO:1200390 (https://orcid.org/0000-0003-0011-764X)
  • MEDGEN:927869 (MONDO:equivalentTo)
  • NANDO:2200340 (https://orcid.org/0000-0003-0011-764X)
  • Orphanet:226298 (MONDO:equivalentTo)
  • icd11.foundation:848364569 (https://orcid.org/0000-0002-4142-7153)
  • UMLS:C4302200 (MONDO:equivalentTo)
Subsets

gard_rare, otar, disease_grouping, rare, nord_rare, ordo_group_of_disorders

IAO 0000233

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

exactMatch

http://identifiers.org/medgen/927869

http://www.orpha.net/ORDO/Orphanet_226298

http://linkedlifedata.com/resource/umls/id/C4302200

http://purl.obolibrary.org/obo/NCIT_C113144

id

MONDO:0016410

seeAlso

https://rarediseases.info.nih.gov/diseases/12280/central-congenital-hypothyroidism

Term relations