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Pituitary deficiency due to empty sella turcica syndrome
disorderSNOMED 715668008CUI C4275064
Overview
Pituitary deficiency due to empty sella turcica syndrome is a disorder.
Auto-generated from clinical reference data. Not a substitute for medical advice.
Signs & Symptoms
Based on Human Phenotype Ontology (HPO) disease-phenotype annotations.
Difficulty getting an erection
Frequent (30-79%)HP:0000802
Headache
Frequent (30-79%)HP:0002315
Light or infrequent menstrual periods
Frequent (30-79%)HP:0000876
Abnormal cerebrospinal fluid morphology
Occasional (5-29%)HP:0002921
Abnormality of mental function
Occasional (5-29%)HP:0011446
ACTH deficiency
Occasional (5-29%)HP:0011748
Autoimmune disorder
Occasional (5-29%)HP:0002960
Decreased response to growth hormone stimulation test
Occasional (5-29%)HP:0000824
Decreased visual acuity
Occasional (5-29%)HP:0007663
Epilepsy
Occasional (5-29%)HP:0001250
Hypopituitarism
Occasional (5-29%)HP:0040075
Precocious puberty
Occasional (5-29%)HP:0000826
Prolactin excess
Occasional (5-29%)HP:0000870
TSH deficient hypothyroidism
Occasional (5-29%)HP:0008245
Visual acuity test abnormality
Occasional (5-29%)HP:0030532
Double vision
Very rare (1-4%)HP:0000651
Hyponatremia
Very rare (1-4%)HP:0002902
Hypotension
Very rare (1-4%)HP:0002615
Neurohypophyseal diabetes insipidus
Very rare (1-4%)HP:0000863
Trigeminal neuralgia
Very rare (1-4%)HP:0100661
Related Conditions
Quick Facts
- SNOMED CT
- 715668008
- UMLS CUI
- C4275064
- Fully Specified Name
- Pituitary deficiency due to empty sella turcica syndrome (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
- HPO Phenotypes
- 20
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.