Search Ontology:
Human Disease

thyroid dyshormonogenesis 5

Term ID
DOID:0112184
Synonyms
  • genetic defect in thyroid hormonogenesis 5
  • TDH5
Definition
A familial thyroid dyshormonogenesis that has_material_basis_in homozygous or compound heterozygous mutation in DUOXA2 on chromosome 15q21.1. https://pubmed.ncbi.nlm.nih.gov/18042646/
References
Ontology
Human Disease   ( DOID:0112184 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Human Gene Zebrafish Ortholog OMIM Term Disease OMIM Phenotype ID
DUOXA1Thyroid dyshormonogenesis 5thyroid dyshormonogenesis 5274900
DUOXA2Thyroid dyshormonogenesis 5thyroid dyshormonogenesis 5274900
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Zebrafish Models
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