Athyreosis is a form of thyroid dysgenesis characterized by complete absence of thyroid tissue that results in primary congenital hypothyroidism, a permanent thyroid deficiency that is present from birth. [ Orphanet:95713 ]
This is just here as a test because I lose it
Term information
database
cross reference
- Orphanet:95713 (MONDO:equivalentTo)
- MEDGEN:155447 (MONDO:equivalentTo)
- UMLS:C0749420 (MONDO:equivalentTo)
- GARD:16842 (MONDO:GARD)
- NANDO:2200331 (https://orcid.org/0000-0003-0011-764X)
Subsets
ordo_disorder, gard_rare, otar, rare, ordo_morphological_anomaly, nord_rare, orphanet_rare
exactMatch
http://identifiers.org/medgen/155447
http://www.orpha.net/ORDO/Orphanet_95713
http://linkedlifedata.com/resource/umls/id/C0749420