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Items: 2

1.

Familial hyperthyroidism due to mutations in TSH receptor

A rare hyperthyroidism characterized by mild to severe hyperthyroidism, presence of goiter, absence of features of autoimmunity, frequent relapses while on treatment and a positive family history. [from ORDO]

MedGen UID:
373154
Concept ID:
C1836706
Disease or Syndrome
2.

Thyroid hyperplasia

Hyperplasia of the thyroid gland. [from HPO]

MedGen UID:
206817
Concept ID:
C1112776
Finding

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