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DO Term : thyroid dyshormonogenesis 2A [DOID:0112186] Disease Ontology
Namespace  disease_ontology Obsolete  false
description  A familial thyroid dyshormonogenesis that has_material_basis_in homozygous or compound heterozygous mutation in TPO on chromosome 2p25.3.
  • synonyms:
  • 274500,
  • OMIM:274500,
  • MESH:C563206,
  • iodide peroxidase deficiency,
  • genetic defect in thyroid hormonogenesis 2A,
  • thyroid peroxidase deficiency,
  • TDH2A
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Disease

Diseases --> Human genes

Diseases --> Mouse genes

Diseases --> Mouse models

Ontology

Ontology Term --> All ancestors

Ontology Term --> All descendants

Ontology Term --> Direct children

Ontology Term --> Direct parents





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