OBO ID: DOID:0112183
Term Name: familial thyroid dyshormonogenesis Search Ontology:
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 familial thyroid dyshormonogenesis PAGES
GENES INVOLVED No data available
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
Your Input Welcome
We welcome your input and comments. Please use this form to recommend updates to the information in ZFIN. We appreciate as much detail as possible and references as appropriate. We will review your comments promptly.
Please check the highlighted fields and try again.
Thank you for submitting comments. Your input has been emailed to ZFIN curators who may contact you if additional information is required.
Oops. Something went wrong. Please try again later.