Overview
Osteosclerosis is a disorder.
Auto-generated from clinical reference data. Not a substitute for medical advice.
Clinical Trials
1
Total Trials
0
Recruiting
0
With Results
Research Evidence
Peer-reviewed studies linked via MeSH term "Osteosclerosis" from the MEDLINE/PubMed database.
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Brain abnormalities, neurodegeneration, and dysosteosclerosis (BANDDOS): new cases, systematic literature review, and associations with CSF1R-ALSP.
[object Object], [object Object], [object Object] et al. · Orphanet J Rare Dis · 2023
[X-ray analysis on 114 patients with moderate endemic skeletal fluorosis by treatment of Guo's Chinese herbal].
[object Object], [object Object], [object Object] et al. · Zhongguo Gu Shang · 2010
PMID: 20575298RCT
FAM20C and FAM20A in normal and ectopic mineralization: A focus on oro-renal syndromes.
[object Object], [object Object], [object Object] et al. · Matrix Biol · 2025
PMID: 41241263Review
Evidence for Thalamic Responsive Neurostimulation in Treatment of Adult and Pediatric Epilepsy.
[object Object], [object Object], [object Object] et al. · Stereotact Funct Neurosurg · 2023
PMID: 36731446Review
TGF-β and BMP Signaling Pathways in Skeletal Dysplasia with Short and Tall Stature.
[object Object], [object Object], [object Object] · Annu Rev Genomics Hum Genet · 2023
PMID: 37624666Review
Modeling CSF-1 receptor deficiency diseases - how close are we?
[object Object], [object Object], [object Object] · FEBS J · 2022
Imaging in osteopetrosis.
[object Object], [object Object], [object Object] · Bone · 2022
PMID: 36116759Review
Redox Implications of Extreme Task Performance: The Case in Driver Athletes.
[object Object] · Cells · 2022
Focus on Osteosclerotic Progression in Primary Myelofibrosis.
[object Object], [object Object], [object Object] et al. · Biomolecules · 2021
FAM20C Overview: Classic and Novel Targets, Pathogenic Variants and Raine Syndrome Phenotypes.
[object Object], [object Object], [object Object] et al. · Int J Mol Sci · 2021
Search all PubMed articles for Osteosclerosis
Research data from MEDLINE/PubMed
Related Conditions
Axial osteosclerosis(child)
Dentin dysplasia with sclerotic bone syndrome(child)
Hyperostosis cranialis interna(child)
Osteosclerotic metaphyseal dysplasia(child)
Autosomal dominant osteopetrosis type 1(child)
Hereditary disorder of musculoskeletal system(parent)
Congenital anomaly of skeletal bone(parent)
Chronic musculoskeletal disorder(parent)
Developmental hereditary disorder(parent)
Quick Facts
- SNOMED CT
- 49347007
- UMLS CUI
- C0029464
- Fully Specified Name
- Osteosclerosis (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
- Clinical Trials
- 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.