Signs & Symptoms
Based on Human Phenotype Ontology (HPO) disease-phenotype annotations.
Abnormal skeletal development
Very frequent (80-99%)HP:0002652
Arthritic pain
Very frequent (80-99%)HP:0002829
Bone overgrowth
Very frequent (80-99%)HP:0100774
Bone pain
Very frequent (80-99%)HP:0002653
Calcification of muscle tissue
Very frequent (80-99%)HP:0011987
Cranial nerve paralysis
Very frequent (80-99%)HP:0006824
Increased bone mineral density
Very frequent (80-99%)HP:0011001
Lymphoedema
Very frequent (80-99%)HP:0001004
Muscle wasting
Very frequent (80-99%)HP:0003202
Skeletal anomalies
Very frequent (80-99%)HP:0000924
Stiff joint
Very frequent (80-99%)HP:0001387
Undergrowth
Very frequent (80-99%)HP:0001508
Left and right leg differ in length or width
Frequent (30-79%)HP:0100559
Unequal size of arms
Frequent (30-79%)HP:0100560
Atypical scarring
Occasional (5-29%)HP:0000987
Joint inflammation
Occasional (5-29%)HP:0001369
Peripheral arteriovenous fistula
Occasional (5-29%)HP:0100784
Related Conditions
Mixed sclerosing bone dystrophy(child)
Melorheostosis of spine(child)
Melorheostosis of right foot(child)
Melorheostosis of left foot(child)
Melorheostosis of right lower leg(child)
Melorheostosis of left lower leg(child)
Melorheostosis of humerus(child)
Melorheostosis of femur(child)
Melorheostosis of skull(child)
Melorheostosis of rib(child)
Melorheostosis of bone of hand(child)
Melorheostosis of forearm(child)
Melorheostosis of shoulder region(child)
Melorheostosis of sternum(child)
Melorheostosis of ankle(child)
Dysplasia with increased bone density(parent)
Congenital anomaly of skeletal bone(parent)
Quick Facts
- SNOMED CT
- 44697002
- UMLS CUI
- C0025239
- Fully Specified Name
- Melorheostosis (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
- HPO Phenotypes
- 17
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.