Search Ontology:
Human Disease

familial thyroid dyshormonogenesis

Term ID
DOID:0112183
Synonyms
Definition
A congenital hypothyroidism characterized by thyroid hormone deficiency that is present from birth and results from defects in thyroid hormone synthesis. https://pubmed.ncbi.nlm.nih.gov/15863666/
References
  • ORDO:95716
Ontology
Human Disease   ( DOID:0112183 )
Relationships
is a type of
has subtype
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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