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.
Prune belly syndrome
Very frequent (80-99%)
Ehlers-Danlos syndrome, type 3
Occasional (5-29%)
Hypogonadotropic hypogonadism
Very frequent (80-99%)
Polyostotic fibrous dysplasia of bone
Occasional (5-29%)
Werner syndrome
Frequent (30-79%)
Testicular regression syndrome
Very frequent (80-99%)
3-Oxo-5 alpha-steroid delta 4-dehydrogenase deficiency
Very frequent (80-99%)
Sotos' syndrome
Very rare (1-4%)
Steinert myotonic dystrophy syndrome
Occasional (5-29%)
Pulmonary alveolar microlithiasis
Very rare (1-4%)
Hypogonadism with anosmia
Very frequent (80-99%)
Multiple lentigines syndrome
Frequent (30-79%)
Deficiency of steroid 17-alpha-hydroxylase
Frequent (30-79%)
Progressive cerebellar ataxia with hypogonadism
Very frequent (80-99%)
Bulbospinal neuronopathy
Very frequent (80-99%)
Young's syndrome
Very frequent (80-99%)
Clastothrix
Berlin syndrome
Very frequent (80-99%)
BIDS brittle hair-impaired intellect-decreased fertility-short stature syndrome
Ulnar mammary syndrome
Frequent (30-79%)
3-M syndrome
Occasional (5-29%)
Atypical Werner syndrome
Very frequent (80-99%)
Congenital adrenal hyperplasia due to cytochrome P450 oxidoreductase deficiency
Frequent (30-79%)
Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency
Frequent (30-79%)
Hypergonadotropic hypogonadism with cataract syndrome
Very frequent (80-99%)
Quick Facts
- SNOMED CT
- 17276009
- UMLS CUI
- C0729353
- Fully Specified Name
- Decreased fertility (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.