Thyroid hypoplasia is a form of thyroid dysgenesis characterized by incomplete development of the thyroid gland that results in primary congenital hypothyroidism, a permanent thyroid deficiency that is present from birth. [ Orphanet:95720 ]
This is just here as a test because I lose it
Term information
database
cross reference
- MedDRA:10065938 (Orphanet:95720/e)
- UMLS:C0151516 (MONDO:equivalentTo)
- MEDGEN:57720 (MONDO:equivalentTo)
- GARD:8426 (MONDO:GARD)
- Orphanet:95720 (MONDO:equivalentTo)
Subsets
ordo_disorder, gard_rare, otar, rare, ordo_morphological_anomaly, nord_rare, orphanet_rare
exactMatch
http://linkedlifedata.com/resource/umls/id/C0151516
http://identifiers.org/medgen/57720
http://www.orpha.net/ORDO/Orphanet_95720