1220575002: Fetal encasement syndrome (disorder)

• SNOMED CT Concept\constatation clinique\...
• \constatation à propos de la structure d'un membre\affection d'une extrémité\Fetal encasement syndrome (disorder)
• \Foetal finding\Fetal disorder\Disorder of fetal structure\Multiple anomalies of fetus (disorder)\Fetal encasement syndrome (disorder)
• \Disease\Genetic disease\maladie héréditaire\Developmental hereditary disorder\Fetal encasement syndrome (disorder)
• \Disease\Genetic disease\maladie héréditaire\Autosomal hereditary disorder\Autosomal recessive hereditary disorder\Fetal encasement syndrome (disorder)
• \Disease\Disorder of fetus or newborn (disorder)\Fetal disorder\Disorder of fetal structure\Multiple anomalies of fetus (disorder)\Fetal encasement syndrome (disorder)
• \Disease\affection d'une extrémité\Fetal encasement syndrome (disorder)
• \Disease\trouble du développement\Disorder of fetal structure\Multiple anomalies of fetus (disorder)\Fetal encasement syndrome (disorder)
• \Disease\trouble du développement\Developmental hereditary disorder\Fetal encasement syndrome (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-May 2022. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
5045227017	Cocoon syndrome	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
5045228010	Foetal encasement syndrome	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
5045229019	Fetal encasement syndrome (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
5045230012	Fetal encasement syndrome	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
5045238017	A rare lethal developmental defect during embryogenesis with characteristics of severe fetal malformations. These malformations include craniofacial dysmorphism (abnormal cyst in the cranial region, hypoplastic eyeballs, two orifices in the nasal region separated by a nasal septum, abnormal orifice replacing the mouth), omphalocele and immotile hypoplastic limbs encased under an abnormal, transparent membrane-like skin. Additional features include absence of adnexal structures of the skin on the outer aspect of the limbs, as well as underdeveloped skeletal muscles and bones. Association with tetralogy of Fallot, horseshoe kidneys, diaphragm and lung lobulation defects is reported.	en	Definition	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core

Expanded Value Set

This concept is not in any reference sets

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