Treatments & Interventions
Related Conditions
Osteopetrosis - delayed type(child)
Osteopetrosis - intermediate type(child)
Carbonic anhydrase II deficiency(child)
Infantile malignant osteopetrosis(child)
Osteochondrodysplasia with osteopetrosis(child)
Transient infantile osteopetrosis(child)
Anhidrotic ectodermal dysplasia, immunodeficiency, osteopetrosis, lymphedema syndrome(child)
Infantile osteopetrosis with neuroaxonal dysplasia syndrome(child)
Autosomal dominant osteopetrosis type 2(child)
Autosomal dominant osteopetrosis type 1(child)
COMMAD (coloboma, osteopetrosis, microphthalmia, macrocephaly, albinism, deafness) syndrome(child)
Congenital anomaly of skeletal bone(parent)
Hereditary disorder of musculoskeletal system(parent)
Chronic musculoskeletal disorder(parent)
Developmental hereditary disorder(parent)
Quick Facts
- SNOMED CT
- 1926006
- UMLS CUI
- C0029454
- Fully Specified Name
- Osteopetrosis (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
- Known Treatments
- 1
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.