Overview
POIKTMP syndrome is a disorder.
Auto-generated from clinical reference data. Not a substitute for medical advice.
Related Conditions
Autosomal dominant hereditary disorder(parent)
Weary-Kindler syndrome(parent)
Fibrosis of lung(parent)
Chronic skin disease(parent)
Connective tissue hereditary disorder(parent)
Hereditary disorder of musculoskeletal system(parent)
Chronic musculoskeletal disorder(parent)
Disease of skeletal muscle(parent)
Tendon contracture(parent)
Chronic lung disease(parent)
Quick Facts
- SNOMED CT
- 771306007
- UMLS CUI
- C4749823
- Fully Specified Name
- Hereditary fibrosing poikiloderma, tendon contractures, myopathy, pulmonary fibrosis 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.