FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term fetal encasement syndrome ID (Ontology) DOID:0060647 (Human Disease)
Definition A syndrome that has_material_basis_in homozygous mutation in the CHUK gene on chromosome 10q24 and is characterized by multiple fetal malformations including defective face and seemingly absent limbs, which are bound to the trunk and encased under the skin.
Also Known As "cocoon syndrome"
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 Genes
 fetal encasement syndrome       1
 for disease ribbon | fetal encasement syndrome       1
 model of | fetal encasement syndrome       1
Spanning Tree (Parents/Children)
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autosomal genetic disease
 |__autosomal recessive disease__
disease                          |
 |__syndrome_____________________|
                                 fetal encasement syndrome  1 rec.
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Is a autosomal recessive disease
syndrome
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Synonyms
  • "cocoon syndrome" EXACT
Secondary IDs
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MIM:613630
ORDO:465824