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Lung fibrosis, immunodeficiency, 46,XX gonadal dysgenesis syndrome
disorderSNOMED 721977007CUI C4302919
Overview
Lung fibrosis, immunodeficiency, 46,XX gonadal dysgenesis syndrome is a disorder.
Auto-generated from clinical reference data. Not a substitute for medical advice.
Related Conditions
Fibrosis of lung(parent)
Pure gonadal dysgenesis 46,XX(parent)
Autosomal recessive severe combined immunodeficiency disease(parent)
Hereditary disorder of endocrine system(parent)
Reproductive system hereditary disorder(parent)
Developmental hereditary disorder(parent)
T-B+ SCID - T-cell negative B-cell positive severe combined immunodeficiency(parent)
Quick Facts
- SNOMED CT
- 721977007
- UMLS CUI
- C4302919
- Fully Specified Name
- Lung fibrosis, immunodeficiency, 46,XX gonadal dysgenesis syndrome (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
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.