Familial gestational hyperthyroidism

Orpha code: 99819OMIM code: 603373

Definition

A rare genetic hyperthyroidism characterized by hyperemesis gravidarum associated with hyperthyroidism due to hypersensitivity of the thyrotropin receptor to chorionic gonadotropin, in the absence of abnormally high serum chorionic gonadotropin levels. Clinical manifestations include severe nausea, vomiting, weight loss, tachycardia, excessive sweating, and hand tremor, but no signs of ophthalmopathy.

Disease data
Classification

Disease

ORPHA code
99819
OMIM code
603373
ICD10 code
E05.8
ICD11 code
-

No additional description.

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