Signs & Symptoms
Based on Human Phenotype Ontology (HPO) disease-phenotype annotations.
Gonadotropin excess
HP:0000837
Primary hypogonadism
HP:0000815
Related Conditions
Leydig cell hypoplasia due to complete LH receptor inactivation(child)
Leydig cell hypoplasia due to partial luteinizing hormone receptor inactivation(child)
Congenital anomaly of endocrine testis(parent)
Congenital connective tissue disorder(parent)
Connective tissue hereditary disorder(parent)
Reproductive system hereditary disorder(parent)
Recessive hereditary disorder (autosomal)(parent)
Congenital hypoplasia of testis(parent)
Hereditary disorder of endocrine system(parent)
Developmental hereditary disorder(parent)
Quick Facts
- SNOMED CT
- 56212008
- UMLS CUI
- C0266432
- Fully Specified Name
- Leydig cell agenesis (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
- HPO Phenotypes
- 2
Medical Disclaimer
This information is for educational purposes only and does not constitute medical advice, diagnosis, or treatment. Always consult with a qualified healthcare provider regarding any medical condition or treatment plan.
Clinical content is derived from the SNOMED CT clinical ontology and curated medical knowledge graphs.