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DOID:0050328 - congenital hypothyroidism
Disease Ontology Definition:A hypothyroidism that is present at birth.
Synonyms: cretinism,
Xenbase Genes
![Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries](img/icons/info1.png)
MONDO:0018612 - congenital hypothyroidism |
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
hypothyroidism (is_a),
physical disorder (is_a)