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Metadata
ID DOID:0112189
Name thyroid dyshormonogenesis 6
Definition A familial thyroid dyshormonogenesis that has_material_basis_in homozygous or compound heterozygous mutation in DUOX2 on chromosome 15q21.1.
https://pubmed.ncbi.nlm.nih.gov/12110737/
Xrefs

MESH:C564608

OMIM:607200

Synonyms

genetic defect in thyroid hormonogenesis 6 [EXACT]

TDH6 [EXACT]

Parent Relationships

is_a familial thyroid dyshormonogenesis

is_a autosomal recessive disease

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