Non-acquired panhypopituitarism

Orpha code: 90695OMIM code: 312000

Definition

A rare genetic pituitary disease characterized by variable deficiency of all hormones produced in the anterior lobe of the pituitary gland. Clinical manifestations include hypothyroidism, hypogonadism, growth retardation and short stature, and secondary adrenal insufficiency. Age of onset is variable. Signs and symptoms usually develop gradually, and loss of the different hormones is often sequential.

Disease data
Classification

Disease

Synonyms
Genetic panhypopituitarism
Genetic panhypopituitarism
ORPHA code
90695
OMIM code
312000
ICD10 code
E23.0
ICD11 code
5A61.0

No additional description.

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