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WormBase Tree Display for DO_term: DOID:0112189

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Name Class

DOID:0112189Namethyroid dyshormonogenesis 6
StatusValid
DefinitionA familial thyroid dyshormonogenesis that has_material_basis_in homozygous or compound heterozygous mutation in DUOX2 on chromosome 15q21.1.
SynonymExactTDH6
genetic defect in thyroid hormonogenesis 6
ParentIs_aDOID:0050737
DOID:0112183
DB_infoDatabaseOMIMdisease607200
Attribute_ofGene_by_orthologyWBGene00000253
WBGene00018771