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 ]
Term information
- GARD:16844 (MONDO:GARD)
- MEDGEN:868785 (MONDO:equivalentTo)
- UMLS:C4023190 (MONDO:equivalentTo)
- Orphanet:95719 (MONDO:equivalentTo)
- SCTID:715734006 (MONDO:equivalentTo)
gard_rare, ordo_disorder, otar, rare, ordo_morphological_anomaly, nord_rare, orphanet_rare
http://identifiers.org/snomedct/715734006
http://www.orpha.net/ORDO/Orphanet_95719
http://identifiers.org/medgen/868785
http://linkedlifedata.com/resource/umls/id/C4023190