Clinical Trials
2
Total Trials
2
Recruiting
0
With Results
Signs & Symptoms
Based on Human Phenotype Ontology (HPO) disease-phenotype annotations.
Abnormal skeletal development
Very frequent (80-99%)HP:0002652
Abnormal skin colour
Very frequent (80-99%)HP:0001000
Abnormal subcutaneous fat tissue distribution
Very frequent (80-99%)HP:0007552
Abnormal vertebral bodies
Very frequent (80-99%)HP:0003312
Abnormalities of the fingers
Very frequent (80-99%)HP:0001167
Arteriovenous malformation
Very frequent (80-99%)HP:0100026
Asymmetry of the thorax
Very frequent (80-99%)HP:0001555
Cachexia
Very frequent (80-99%)HP:0004326
Capillary hemangioma
Very frequent (80-99%)HP:0005306
Cobb angle greater than ten degrees
Very frequent (80-99%)HP:0002650
Decreased muscle mass
Very frequent (80-99%)HP:0003199
Diffusely thickened skin
Very frequent (80-99%)HP:0001072
Disproportionate tall stature
Very frequent (80-99%)HP:0001519
Epidermal nevus
Very frequent (80-99%)HP:0010816
Fatty lump
Very frequent (80-99%)HP:0012032
General overgrowth
Very frequent (80-99%)HP:0001548
Hunched back
Very frequent (80-99%)HP:0002808
Increased ossification of cranial bones
Very frequent (80-99%)HP:0004437
Irregular hyperpigmentation
Very frequent (80-99%)HP:0007400
Left and right leg differ in length or width
Very frequent (80-99%)HP:0100559
Lymphangioma
Very frequent (80-99%)HP:0100764
Macrodactyly
Very frequent (80-99%)HP:0004099
Nevocellular nevi
Very frequent (80-99%)HP:0000995
Subcutaneous nodule
Very frequent (80-99%)HP:0001482
Unequal size of arms
Very frequent (80-99%)HP:0100560
Uneven or disproportionate growth of one body part compared to another
Very frequent (80-99%)HP:0100555
Vascular skin abnormality
Very frequent (80-99%)HP:0011276
Blood clot in artery of lung
Frequent (30-79%)HP:0002204
Bone overgrowth
Frequent (30-79%)HP:0100774
Bronchogenic cyst
Frequent (30-79%)HP:0100730
Related Conditions
Port-wine stain in proteus syndrome(child)
Neuroectodermal dysplasia(parent)
Hereditary disorder of the integument(parent)
Hereditary disorder of nervous system(parent)
Congenital hamartoma of skin(parent)
Skeletal dysplasia(parent)
Hereditary disorder of musculoskeletal system(parent)
Multiple malformation syndrome with early overgrowth(parent)
Hereditary neoplastic syndrome(parent)
Developmental hereditary disorder(parent)
Congenital anomaly of nervous system(parent)
Quick Facts
- SNOMED CT
- 23150001
- UMLS CUI
- C0085261
- Fully Specified Name
- Proteus syndrome (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
- HPO Phenotypes
- 30
- Clinical Trials
- 2
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.