familial thyroid dyshormonogenesis Disease Ontology Browser

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Disease Ontology Browser

familial thyroid dyshormonogenesis (DOID:0112183)
Alliance: disease page
Alt IDs: ORDO:95716
Definition: A congenital hypothyroidism characterized by thyroid hormone deficiency that is present from birth and results from defects in thyroid hormone synthesis.

Contributing Projects: Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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