Overview
Clinical overview and emergency guidance are pending physician authorship. Graph-derived data (ontology codes, linked conditions, diagnostic biomarkers) is available below.
Associated Conditions
Conditions associated with this symptom based on HPO disease-phenotype annotations.
Hypercortisolism due to nonpituitary tumor
Occasional (5-29%)
Isolated lutropin deficiency
Panhypopituitarism
Very frequent (80-99%)
Asherman syndrome
Frequent (30-79%)
Pseudohypoparathyroidism type I A
Occasional (5-29%)
Acromegaly
Occasional (5-29%)
Acquired generalized lipodystrophy
Very rare (1-4%)
Prader-Willi syndrome
Frequent (30-79%)
Gonadal dysgenesis with auditory dysfunction, autosomal recessive inheritance
Occasional (5-29%)
Deficiency of uridyl transferase
Frequent (30-79%)
Pituitary dependent hypercortisolism
Occasional (5-29%)
Progressive cerebellar ataxia with hypogonadism
Frequent (30-79%)
Glycogen phosphorylase kinase deficiency
Occasional (5-29%)
Polycystic ovary syndrome
Hyperprolactinemia
Frequent (30-79%)
Sheehan's syndrome
Very frequent (80-99%)
Pituitary apoplexy
Frequent (30-79%)
Berardinelli's syndrome
Very rare (1-4%)
Postpartum hypopituitarism
Very frequent (80-99%)
Deficiency of UTP-hexose-1-phosphate uridylyltransferase
Frequent (30-79%)
Fowler's syndrome
Occasional (5-29%)
Mowat-Wilson syndrome
Very rare (1-4%)
Pituitary deficiency due to empty sella turcica syndrome
Frequent (30-79%)
Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency
Frequent (30-79%)
Pseudohypoparathyroidism type 1C
Occasional (5-29%)
Quick Facts
- SNOMED CT
- 52073004
- UMLS CUI
- C0028949
- Fully Specified Name
- Oligomenorrhea (finding)
- Associated Conditions
- 25
- Diagnostic Tests
- 0
This information is for educational purposes only. If you are experiencing symptoms, please consult a healthcare provider for proper evaluation and diagnosis.