Signs & Symptoms
Based on Human Phenotype Ontology (HPO) disease-phenotype annotations.
Decreased circulating follicle stimulating hormone concentration
Always present (100%)HP:0030341
Decreased circulating luteinizing hormone level
Always present (100%)HP:0030344
Decreased thyrotropin level
Always present (100%)HP:0031098
Reduced circulating growth hormone concentration
Always present (100%)HP:0034323
ACTH deficiency
Very frequent (80-99%)HP:0011748
ACTH deficient adrenal insufficiency
Very frequent (80-99%)HP:0011735
Chronic extreme exhaustion
Very frequent (80-99%)HP:0012432
Hypocortisolism
Very frequent (80-99%)HP:0008163
Light or infrequent menstrual periods
Very frequent (80-99%)HP:0000876
Panhypopituitarism
Very frequent (80-99%)HP:0000871
Secondary growth hormone deficiency
Very frequent (80-99%)HP:0008240
Abnormal size of pituitary gland
Frequent (30-79%)HP:0012504
Amenorrhea
Frequent (30-79%)HP:0000141
Blurred vision
Frequent (30-79%)HP:0000622
Central adrenal insufficiency
Frequent (30-79%)HP:0011734
Decrease in blood pressure upon standing up
Frequent (30-79%)HP:0001278
Decreased female sex drive
Frequent (30-79%)HP:0030018
Decreased serum estradiol
Frequent (30-79%)HP:0008214
Decreased sexual hair
Frequent (30-79%)HP:0002225
Difficulty getting an erection
Frequent (30-79%)HP:0000802
Dyspareunia
Frequent (30-79%)HP:0030016
Headache
Frequent (30-79%)HP:0002315
Hyposthenuria
Frequent (30-79%)HP:0003158
Low blood sugar
Frequent (30-79%)HP:0001943
Nausea
Frequent (30-79%)HP:0002018
Normochromic anaemia
Frequent (30-79%)HP:0001895
Paleness
Frequent (30-79%)HP:0000980
Pituitary gonadotropin deficiency
Frequent (30-79%)HP:0008213
Progressive visual field defects
Frequent (30-79%)HP:0007987
Reduced circulating prolactin concentration
Frequent (30-79%)HP:0008202
Related Conditions
Panhypopituitarism - anterior and posterior(child)
Panhypopituitarism - X-linked(child)
Prepuberal panhypopituitarism(child)
Idiopathic panhypopituitarism(child)
Post-birth injury panhypopituitarism(child)
Post-infarction panhypopituitarism(child)
Non-acquired combined pituitary hormone deficiency, deafness, rigid cervical spine syndrome(child)
Hypopituitarism(parent)
Disorder of anterior pituitary(parent)
Quick Facts
- SNOMED CT
- 32390006
- UMLS CUI
- C0242343
- Fully Specified Name
- Panhypopituitarism (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
- HPO Phenotypes
- 30
Medical Disclaimer
This information is for educational purposes only and does not constitute medical advice, diagnosis, or treatment. Always consult with a qualified healthcare provider regarding any medical condition or treatment plan.
Clinical content is derived from the SNOMED CT clinical ontology and curated medical knowledge graphs.