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.
Bardet-Biedl syndrome
Occasional (5-29%)
Glucose-6-phosphate transport defect
Frequent (30-79%)
Polyostotic fibrous dysplasia of bone
Occasional (5-29%)
Alstrom syndrome
Occasional (5-29%)
Primary ovarian failure
Acrodysostosis
Occasional (5-29%)
Isolated prolactin deficiency
Occasional (5-29%)
Deficiency of steroid 11-beta-hydroxylase
Frequent (30-79%)
Deficiency of steroid 17-alpha-hydroxylase
Frequent (30-79%)
Prolactinoma
Very frequent (80-99%)
Glycogen phosphorylase kinase deficiency
Occasional (5-29%)
Premature ovarian failure
Thyrotroph adenoma
Frequent (30-79%)
Functionless pituitary adenoma
Frequent (30-79%)
Familial isolated pituitary adenoma
Autoinflammation, lipodystrophy and dermatosis syndrome
Occasional (5-29%)
Aromatase excess syndrome
Occasional (5-29%)
Blepharophimosis epicanthus inversus ptosis syndrome
Hypercortisolism due to macronodular adrenal hyperplasia
Frequent (30-79%)
Hidrotic ectodermal dysplasia Halal type
Frequent (30-79%)
McCune Albright syndrome
Occasional (5-29%)
Hyperandrogenism due to cortisone reductase deficiency
Frequent (30-79%)
Glycogen storage disease due to liver and muscle glycogen phosphorylase kinase deficiency
Occasional (5-29%)
Cockayne syndrome type 1
Polyembryoma
Very rare (1-4%)
Quick Facts
- SNOMED CT
- 80182007
- UMLS CUI
- C0156404
- Fully Specified Name
- Irregular periods (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.