pituitary deficiency due to empty sella turcica syndrome
MONDO:0019617Mondo
Findings
No curated finding names pituitary deficiency due to empty sella turcica syndrome yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Features
20 features
What the disease is reported to present with, and how often among people who have it — never how often a feature means the disease. HPO, annotations 2026-09-02.
- HeadacheHPOHP:0002315
- Frequent (30% to 79% of cases)
- ImpotenceHPOHP:0000802
- Frequent (30% to 79% of cases)
- OligomenorrheaHPOHP:0000876
- Frequent (30% to 79% of cases)
- Abnormal cerebrospinal fluid morphologyHPOHP:0002921
- Occasional (5% to 29% of cases)
- Abnormality of mental functionHPOHP:0011446
- Occasional (5% to 29% of cases)
- Adrenocorticotropic hormone deficiencyHPOHP:0011748
- Occasional (5% to 29% of cases)
- AutoimmunityHPOHP:0002960
- Occasional (5% to 29% of cases)
- Decreased response to growth hormone stimulation testHPOHP:0000824
- Occasional (5% to 29% of cases)
- HypopituitarismHPOHP:0040075
- Occasional (5% to 29% of cases)
- Increased circulating prolactin concentrationHPOHP:0000870
- Occasional (5% to 29% of cases)
- Pituitary hypothyroidismHPOHP:0008245
- Occasional (5% to 29% of cases)
- Precocious pubertyHPOHP:0000826
- Occasional (5% to 29% of cases)
Reported absent (1)
- Pituitary adenomaHPOHP:0002893
Show the remaining 8
- Reduced visual acuityHPOHP:0007663
- Occasional (5% to 29% of cases)
- SeizureHPOHP:0001250
- Occasional (5% to 29% of cases)
- Visual acuity test abnormalityHPOHP:0030532
- Occasional (5% to 29% of cases)
- Central diabetes insipidusHPOHP:0000863
- Very rare (1% to 4% of cases)
- DiplopiaHPOHP:0000651
- Very rare (1% to 4% of cases)
- HyponatremiaHPOHP:0002902
- Very rare (1% to 4% of cases)
Where it sits
- A kind of
Other names
1 name
Resolves to: pituitary deficiency due to empty sella turcica syndrome
- Also called
- hypopituitarism due to empty sella turcica syndrome