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DO Term : nonautoimmune hyperthyroidism [DOID:0081101] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

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.

synonyms:
609152,
Congenital nonautoimmune hyperthyroidism,
OMIM:609152,
ORDO:424

Disease

Diseases --> Human genes

Diseases --> Mouse genes

Diseases --> Mouse models

Ontology

Ontology Term --> All ancestors

Ontology Term --> All descendants

Ontology Term --> Direct children

Ontology Term --> Direct parents

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