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
Occasional (5-29%)
Isolated lutropin deficiency
Always present (100%)
Ring chromosome 22 syndrome
Frequent (30-79%)
Fanconi pancytopenia syndrome
Occasional (5-29%)
Ring chromosome 21 syndrome
Occasional (5-29%)
Hypogonadotropic hypogonadism
Hereditary hemochromatosis
XXXXY syndrome
Very frequent (80-99%)
Double Y syndrome
Occasional (5-29%)
Juvenile hemochromatosis
3 beta-Hydroxysteroid dehydrogenase deficiency
Occasional (5-29%)
XXXY syndrome
Very frequent (80-99%)
Lowe syndrome
Occasional (5-29%)
Mixed gonadal dysgenesis
Frequent (30-79%)
Gonadal dysgenesis with auditory dysfunction, autosomal recessive inheritance
Occasional (5-29%)
Hypogonadism with anosmia
Cystinosis
Occasional (5-29%)
Young's syndrome
Congenital adrenal hypoplasia, X-linked
Teratoma of testis
Congenital bilateral aplasia of vas deferens
Idiopathic haemochromatosis
Primary haemochromatosis
XXYY syndrome
Very frequent (80-99%)
Yolk sac tumour
Quick Facts
- SNOMED CT
- 48188009
- UMLS CUI
- C0004509
- Fully Specified Name
- Azoospermia (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.