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%)
Double Y syndrome
Occasional (5-29%)
Alstrom syndrome
Occasional (5-29%)
Familial visceral amyloidosis, Ostertag type
Very rare (1-4%)
Oligochiasmic infertility
Always present (100%)
Congenital adrenal hypoplasia, X-linked
Frequent (30-79%)
Odontotrichomelic syndrome
Occasional (5-29%)
Gonadotrophin-secreting pituitary adenoma
Occasional (5-29%)
Congenital bilateral aplasia of vas deferens
Occasional (5-29%)
Proximal myotonic myopathy
Isochromosome 9p
Occasional (5-29%)
Congenital adrenal hyperplasia due to cytochrome P450 oxidoreductase deficiency
Frequent (30-79%)
Growth retardation, alopecia, pseudoanodontia, optic atrophy syndrome
Occasional (5-29%)
Familial male-limited precocious puberty
Occasional (5-29%)
Carney complex
Occasional (5-29%)
Isolated follicle stimulating hormone deficiency
Frequent (30-79%)
Ring chromosome 15 syndrome
Occasional (5-29%)
SOFT syndrome
Pituitary dermoid and epidermoid cysts
Occasional (5-29%)
Generalized glucocorticoid resistance syndrome
Occasional (5-29%)
Saturnine poisoning
Very rare (1-4%)
Quick Facts
- SNOMED CT
- 88311004
- UMLS CUI
- C0868910
- Fully Specified Name
- Oligozoospermia (finding)
- Associated Conditions
- 21
- 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.