Hypopituitarism

Alias:

Pituitary Hypofunction

Deficient Secretion of One or More Pituitary Hormones

Deficient Secretion of All Pituitary Hormones

Postpartum Panhypopituitary Syndrome

Anterior Pituitary Insufficiency

Anterior Pituitary Hypofunction

Prepubertal Panhypopituitarism

Pituitary Hypoadrenocorticism

Pituitary Hormone Deficiency

Pituitary Gland Hypofunction

Pituitary Insufficiency Nos

Panhypopituitarism Syndrome

Postpartum Hypopituitarism

Hyposomatotropic Dwarfism

Hypophyseal Short Stature

Hypopituitarism Syndrome

Juvenile Hypopituitarism

Pituitary Insufficiency

Primary Hypopituitarism

Pituitary Short Stature

Hypopituitary Dwarfism

Hypopituitary Cachexia

Secondary Hypogonadism

Pituitary Hypogonadism

Hypophyseal Dystrophy

Pituitary Infantilism

Pituitary Deficiency

Hypophyseal Dwarfism

Prepubertal Dwarfism

Pituitary Dwarfism

Pituitary Cachexia

Pituitary Failure

Hypohypophysism

Subpituitarism

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Hypopituitarism, also known as pituitary hypofunction, is related to combined pituitary hormone deficiencies, genetic forms and culler-jones syndrome. An important gene associated with Hypopituitarism is TBC1D32 (TBC1 Domain Family Member 32), and among its related pathways/superpathways are Signal Transduction and p70S6K Signaling. The drugs Methyltestosterone and Testosterone enanthate have been mentioned in the context of this disorder. Affiliated tissues include pituitary and thyroid, and related phenotypes are nervous system and homeostasis/metabolism

Related ID：

MALACARDS：HYP083

MESH：D007018

ICD11：292840069/other