OBO ID: DOID:0112184 |
Term Name: | thyroid dyshormonogenesis 5 | Search Ontology: | |
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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/ | ||
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Ontology: | Human Disease ( DOID:0112184 ) |
OTHER thyroid dyshormonogenesis 5 PAGES
ZEBRAFISH MODELS
No data available
PHENOTYPE
No data available
CITATIONS: None
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