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.
Bloom syndrome
Frequent (30-79%)
Polyglandular autoimmune syndrome, type 1
Frequent (30-79%)
Trisomy X syndrome
Occasional (5-29%)
Turner syndrome
Very frequent (80-99%)
Primary ovarian failure
Rothmund-Thomson syndrome
Frequent (30-79%)
Gonadal dysgenesis with auditory dysfunction, autosomal recessive inheritance
Frequent (30-79%)
Deficiency of galactokinase
Occasional (5-29%)
Deficiency of uridyl transferase
Frequent (30-79%)
Microcephaly, normal intelligence and immunodeficiency
Renal dysplasia and retinal aplasia
Frequent (30-79%)
Premature ovarian failure
Carbohydrate-deficient glycoprotein syndrome type I
Addison's disease
Occasional (5-29%)
Deficiency of UTP-hexose-1-phosphate uridylyltransferase
Frequent (30-79%)
Progeroid short stature with pigmented naevi
Vanishing white matter disease
Frequent (30-79%)
Fragile X associated tremor ataxia syndrome
Congenital disorder of glycosylation type Ia
Autoimmune lymphoproliferative syndrome
Very rare (1-4%)
Blepharophimosis epicanthus inversus ptosis syndrome
Familial partial lipodystrophy type 2
Occasional (5-29%)
Atypical Werner syndrome
Very frequent (80-99%)
Fetal diethylstilbestrol syndrome
Very frequent (80-99%)
Sengers syndrome
Frequent (30-79%)
Quick Facts
- SNOMED CT
- 373717006
- UMLS CUI
- C0025322
- Fully Specified Name
- Premature menopause (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.