Thyroid hemiagenesis is a form of thyroid dysgenesis characterized by an absence of half of the thyroid gland that is usually asymptomatic but may result in primary congenital hypothyroidism, a permanent thyroid deficiency that is present from birth. [ Orphanet:95719 ]

This is just here as a test because I lose it

Term information

database cross reference
  • GARD:16844 (MONDO:GARD)
  • MEDGEN:868785 (MONDO:equivalentTo)
  • UMLS:C4023190 (MONDO:equivalentTo)
  • Orphanet:95719 (MONDO:equivalentTo)
  • SCTID:715734006 (MONDO:equivalentTo)
Subsets

gard_rare, ordo_disorder, otar, rare, ordo_morphological_anomaly, nord_rare, orphanet_rare

exactMatch

http://identifiers.org/snomedct/715734006

http://www.orpha.net/ORDO/Orphanet_95719

http://identifiers.org/medgen/868785

http://linkedlifedata.com/resource/umls/id/C4023190

id

MONDO:0019860

Term relations