Overview
Autosomal recessive osteopetrosis type 7 is a disorder.
Auto-generated from clinical reference data. Not a substitute for medical advice.
Related Conditions
Congenital immunodeficiency disease(parent)
Recessive hereditary disorder (autosomal)(parent)
Hereditary disorder of immune system(parent)
Dysplasia with increased bone density(parent)
Specific antibody deficiency(parent)
Osteochondrodysplasia with osteopetrosis(parent)
Chronic disease of immune structure(parent)
Chronic disease of immune function(parent)
Quick Facts
- SNOMED CT
- 773730002
- UMLS CUI
- C4751205
- Fully Specified Name
- Osteopetrosis hypogammaglobulinemia 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.