789557002: Multiple fetal anomalies (disorder)

SNOMED CT Concept\Clinical finding (finding)\...

\Fetal finding\Fetal disorder\Disorder of fetal structure\Multiple anomalies of fetus

\Disease\Fetal and/or neonatal disorder\Fetal disorder\Disorder of fetal structure\Multiple anomalies of fetus
\Disease\Developmental disorder\Disorder of fetal structure\Multiple anomalies of fetus

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2020. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

3789694011 Multiple anomalies of foetus en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

3789695012 Multiple anomalies of fetus en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

5424607014 Multiple fetal anomalies (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

5424608016 Multiple fetal anomalies en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

7672001000241118 plusieurs anomalies du fœtus fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

7672011000241116 anomalies fœtales multiples fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Multiple anomalies of fetus	Pathological process (attribute)	Pathological developmental process	true	Inferred relationship	Some	1
Multiple anomalies of fetus	Finding site	Fetal structure	false	Inferred relationship	Some	1
Multiple anomalies of fetus	Associated morphology	Morphologically abnormal structure	true	Inferred relationship	Some	1
Multiple anomalies of fetus	Is a	Disorder of fetal structure	true	Inferred relationship	Some
Multiple anomalies of fetus	Occurrence	Fetal period	true	Inferred relationship	Some	1

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Fetal encasement syndrome is a rare, lethal developmental defect during embryogenesis characterized by severe fetal malformations, including 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, horse-shoe kidneys and diaphragm and lung lobulation defects is reported.	Is a	True	Multiple anomalies of fetus	Inferred relationship	Some
Lethal fetal cerebrorenogenitourinary agenesis/hypoplasia syndrome is a rare, genetic developmental defect during embryogenesis malformation syndrome characterized by intrauterine growth restriction, flexion arthrogryposis of all joints, severe microcephaly, renal cystic dysplasia/agenesis/hypoplasia and complex malformations of the brain (cerebral and cerebellar hypoplasia, vermis, corpus callosum and/or occipital lobe agenesis, with or without arhinencephaly), as well as of the genitourinary tract (ureteral agenesis/hypoplasia, uterine hypoplasia and/or vaginal atresia), leading to fetal demise.	Is a	True	Multiple anomalies of fetus	Inferred relationship	Some

This concept is not in any reference sets