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Hypopituitarism
MONDO:0005152A condition of diminution or cessation of secretion of one or more hormones from the anterior pituitary gland. This may result from surgical or radiation ablation, non-secretory pituitary neoplasms, metastatic tumors, infarction, pituitary apoplexy, infiltrative or granulomatous processes, and other conditions.
Also known as: pituitary insufficiency
47 clinical trials for this condition and its sub-types, 5 tagged with Hypopituitarism itself.
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Sub-types of Hypopituitarism
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Combined pituitary hormone deficiencies, genetic form 1 trial · 42 incl. sub-types
9 sub-types
- Isolated congenital growth hormone deficiency 38 trials Sub-types →
- Panhypopituitarism 2 trials Sub-types →
- Congenital isolated adrenocorticotropic hormone deficiency 1 trial
- Pituitary hormone deficiency, combined, 1 1 trial
- Septooptic dysplasia 1 trial Sub-types →
- Non-acquired combined pituitary hormone deficiency with spine abnormalities 0 trials
- Pituitary hormone deficiency, combined or isolated, 8 0 trials
- Pituitary hormone deficiency, combined, 6 0 trials
- Short stature-pituitary and cerebellar defects-small sella turcica syndrome 0 trials
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Acquired pituitary hormone deficiency 0 trials · 1 incl. sub-types
4 sub-types
- Pituitary apoplexy 1 trial
- Iatrogenic or traumatic pituitary deficiency 0 trials
- Late-onset isolated ACTH deficiency 0 trials
- Primary hypophysitis 0 trials Sub-types →
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Kaplowitz-Bodurtha syndrome 0 trials