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.
Panhypopituitarism
Frequent (30-79%)
Sheehan's syndrome
Frequent (30-79%)
Postpartum hypopituitarism
Frequent (30-79%)
Progeroid short stature with pigmented naevi
Very frequent (80-99%)
Frasier syndrome
Very frequent (80-99%)
Pituicytoma
Occasional (5-29%)
Congenital leptin deficiency
Very frequent (80-99%)
CCFDN - congenital cataracts, facial dysmorphism and neuropathy
Congenital adrenal hyperplasia due to cytochrome P450 oxidoreductase deficiency
Frequent (30-79%)
Primary hypergonadotropic hypogonadism and partial alopecia syndrome
Very frequent (80-99%)
46,XY partial gonadal dysgenesis
Very frequent (80-99%)
Isolated follicle stimulating hormone deficiency
Very frequent (80-99%)
Infundibulo panhypophysitis
Frequent (30-79%)
46,XY gonadal dysgenesis, motor and sensory neuropathy syndrome
Very frequent (80-99%)
Anterior pituitary hypophysitis
Frequent (30-79%)
Obesity due to leptin receptor gene deficiency
Very frequent (80-99%)
Diabetes, hypogonadism, deafness, intellectual disability syndrome
Very frequent (80-99%)
3q23 microdeletion syndrome
Occasional (5-29%)
46,XY disorder of sex development due to isolated 17,20-lyase deficiency
Very frequent (80-99%)
46,XX ovarian dysgenesis, short stature syndrome
Always present (100%)
Quick Facts
- SNOMED CT
- 166449002
- UMLS CUI
- C0241011
- Fully Specified Name
- Serum estradiol levels below reference range (finding)
- Associated Conditions
- 20
- 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.