OBO ID: DOID:0112184
Term Name: thyroid dyshormonogenesis 5 Search Ontology:
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)
OTHER thyroid dyshormonogenesis 5 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
DUOXA1 Thyroid dyshormonogenesis 5 274900
DUOXA2 Thyroid dyshormonogenesis 5 274900
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None