Overview
Congenital connective tissue disorder is a disorder.
Auto-generated from clinical reference data. Not a substitute for medical advice.
Related Conditions
Congenital epicardial cyst(child)
Congenital anomaly of cartilage(child)
Inherited cutis laxa(child)
Berardinelli's syndrome(child)
Congenital anomaly of peritoneum(child)
Congenital shortening of tendon(child)
Congenital anomaly of pleural folds(child)
Farber's lipogranulomatosis(child)
Congenital macular corneal dystrophy(child)
Congenital vaginal enterocele(child)
Congenital absence of tendon(child)
Decorin associated congenital stromal corneal dystrophy(child)
Leydig cell agenesis(child)
Congenital syphilitic osteochondritis(child)
Congenital short costocoracoid ligament(child)
Banki syndrome(child)
Congenital nephrotic syndrome, interstitial lung disease, epidermolysis bullosa syndrome(child)
Neonatal Marfan syndrome(child)
16q24.1 microdeletion syndrome(child)
Marfanoid habitus, inguinal hernia, advanced bone age syndrome(child)
Quick Facts
- SNOMED CT
- 363039000
- UMLS CUI
- C0852085
- Fully Specified Name
- Congenital connective tissue disorder (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.