FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term nonautoimmune hyperthyroidism ID (Ontology) DOID:0081101 (Human Disease)
Definition A hyperthyroidism that is characterized by passive transfer of maternal autoantibodies and that has_material_basis_in heterozygous mutation in the thyroid-stimulating hormone receptor gene (TSHR) on chromosome 14q31.
Also Known As "Congenital nonautoimmune hyperthyroidism"
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 Genes
 nonautoimmune hyperthyroidism       1
 for disease ribbon | nonautoimmune hyperthyroidism       1
 model of | nonautoimmune hyperthyroidism       1
Spanning Tree (Parents/Children)
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autosomal genetic disease
 |__autosomal dominant disease__
thyroid gland disease           |
 |__hyperthyroidism_____________|
                                nonautoimmune hyperthyroidism  1 rec.
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Is a autosomal dominant disease
hyperthyroidism
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Synonyms
  • "Congenital nonautoimmune hyperthyroidism" EXACT
Secondary IDs
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MIM:609152
ORDO:424