Search Ontology:
Human Disease

thyroid dyshormonogenesis 2A

Term ID
DOID:0112186
Synonyms
  • genetic defect in thyroid hormonogenesis 2A
  • iodide peroxidase deficiency
  • TDH2A
  • thyroid peroxidase deficiency
Definition
A familial thyroid dyshormonogenesis that has_material_basis_in homozygous or compound heterozygous mutation in TPO on chromosome 2p25.3. https://pubmed.ncbi.nlm.nih.gov/1401057/
References
Ontology
Human Disease   ( DOID:0112186 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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