Overview
Neonatal Marfan syndrome is a disorder.
Auto-generated from clinical reference data. Not a substitute for medical advice.
Signs & Symptoms
Based on Human Phenotype Ontology (HPO) disease-phenotype annotations.
Mitral regurgitation
Always present (100%)HP:0001653
Pulmonary emphysema
Always present (100%)HP:0002097
Tricuspid regurgitation
Always present (100%)HP:0005180
Abnormality of cardiac ventricle
Very frequent (80-99%)HP:0001713
Arachnodactyly
Very frequent (80-99%)HP:0001166
Ascending tubular aorta aneurysm
Very frequent (80-99%)HP:0004970
Atrophy of fat
Very frequent (80-99%)HP:0100578
Birth weight less than 10th percentile
Very frequent (80-99%)HP:0001518
Cardiac murmur
Very frequent (80-99%)HP:0030148
Cardiovascular disease
Very frequent (80-99%)HP:0001626
Decreased testicular size
Very frequent (80-99%)HP:0008734
Feeding difficulties
Very frequent (80-99%)HP:0011968
Flexion contractures
Very frequent (80-99%)HP:0001371
Hypoxemia
Very frequent (80-99%)HP:0012418
Increased corneal diameter
Very frequent (80-99%)HP:0000485
Increased length of toes
Very frequent (80-99%)HP:0010511
Iridodonesis
Very frequent (80-99%)HP:0100693
Lens dislocation
Very frequent (80-99%)HP:0001083
Long fingers
Very frequent (80-99%)HP:0100807
Loose skin
Very frequent (80-99%)HP:0000973
Mitral valve prolapse
Very frequent (80-99%)HP:0001634
Narrow cranium shape
Very frequent (80-99%)HP:0000268
No development of motor milestones
Very frequent (80-99%)HP:0001270
Pectus carinatum
Very frequent (80-99%)HP:0000768
Respiratory distress, neonatal
Very frequent (80-99%)HP:0002643
Severe myopia
Very frequent (80-99%)HP:0011003
Talipes calcaneovarus
Very frequent (80-99%)HP:0008124
Thumb-in-palm pattern
Very frequent (80-99%)HP:0001181
Tricuspid valve prolapse
Very frequent (80-99%)HP:0001704
Wide thorax
Very frequent (80-99%)HP:0100625
Related Conditions
Congenital anomaly of cardiovascular system(parent)
Marfan's syndrome(parent)
Multiple malformation syndrome with facial defects as major feature(parent)
Cardiovascular system hereditary disorder(parent)
Congenital connective tissue disorder(parent)
Neonatal cardiovascular disorder(parent)
Developmental hereditary disorder(parent)
Quick Facts
- SNOMED CT
- 763839005
- UMLS CUI
- C4016054
- Fully Specified Name
- Neonatal Marfan syndrome (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
- HPO Phenotypes
- 30
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.