Overview
Cocoon 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.
Abnormal nasal morphology
Always present (100%)HP:0005105
Abnormally small eyeball
Always present (100%)HP:0000568
Absent bone maturation of skullcap
Always present (100%)HP:0005623
Absent stratum granulosum of epidermis
Always present (100%)HP:0025815
Cerebral cystic malformation
Always present (100%)HP:0010576
Cleft lip, cleft palate
Always present (100%)HP:0000202
Hypoplasia involving bones of the lower limbs
Always present (100%)HP:0009816
Hypoplasia involving bones of the upper limbs
Always present (100%)HP:0009824
Less than 10 fetal movements in 12 hours
Always present (100%)HP:0001558
Lung segmentation defects
Always present (100%)HP:0002101
Omphalocoele
Always present (100%)HP:0001539
Scoliosis
Always present (100%)HP:0002650
Thin skin
Always present (100%)HP:0000963
Underdeveloped muscles
Always present (100%)HP:0009004
Bilateral trilobed lung
Frequent (30-79%)HP:0011861
Diaphragmatic hernia
Frequent (30-79%)HP:0000776
Horseshoe kidney
Frequent (30-79%)HP:0000085
Tetrology of fallot
Frequent (30-79%)HP:0001636
Quick Facts
- SNOMED CT
- 1220575002
- UMLS CUI
- C3150891
- Fully Specified Name
- Fetal encasement syndrome (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
- HPO Phenotypes
- 18
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.