716106000: Limb body wall complex (disorder)

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

\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Disorder of abdominopelvic segment of trunk\Congenital anomaly of lower trunk\Limb body wall complex (disorder)
\Finding of trunk structure\Disorder of trunk (disorder)\Disorder of abdominopelvic segment of trunk\Congenital anomaly of lower trunk\Limb body wall complex (disorder)
\Finding of trunk structure\Disorder of trunk (disorder)\Congenital anomaly of trunk\Congenital anomaly of lower trunk\Limb body wall complex (disorder)

\Disease\Disorder of body wall (disorder)\Congenital anomaly of body wall\Limb body wall complex (disorder)
\Disease\Disorder of trunk (disorder)\Disorder of abdominopelvic segment of trunk\Congenital anomaly of lower trunk\Limb body wall complex (disorder)
\Disease\Disorder of trunk (disorder)\Congenital anomaly of trunk\Congenital anomaly of lower trunk\Limb body wall complex (disorder)
\Disease\Congenital disease (disorder)\Congenital malformation\Congenital malformation syndrome (disorder)\Multiple system malformation syndrome\Multiple malformation syndrome with limb defect as major feature\Limb body wall complex (disorder)
\Disease\Congenital disease (disorder)\Congenital malformation\Congenital anomaly of body wall\Limb body wall complex (disorder)
\Disease\Congenital disease (disorder)\Congenital malformation\Congenital abnormality of lower limb and pelvic girdle\Congenital anomaly of lower trunk\Limb body wall complex (disorder)
\Disease\Congenital disease (disorder)\Congenital malformation\Congenital anomaly of trunk\Congenital anomaly of lower trunk\Limb body wall complex (disorder)
\Disease\Developmental disorder\Congenital malformation\Congenital malformation syndrome (disorder)\Multiple system malformation syndrome\Multiple malformation syndrome with limb defect as major feature\Limb body wall complex (disorder)
\Disease\Developmental disorder\Congenital malformation\Congenital anomaly of body wall\Limb body wall complex (disorder)
\Disease\Developmental disorder\Congenital malformation\Congenital abnormality of lower limb and pelvic girdle\Congenital anomaly of lower trunk\Limb body wall complex (disorder)
\Disease\Developmental disorder\Congenital malformation\Congenital anomaly of trunk\Congenital anomaly of lower trunk\Limb body wall complex (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2016. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

3304753015 Limb body wall complex (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

3304754014 Limb body wall complex en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

3304755010 LBWC (limb body wall complex) syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core

3304756011 Limb body wall complex (LBWC) is a syndrome with features of severe multiple congenital anomalies. Clinical manifestations vary widely and include limb defects and visceral malformations, spinal abnormalities, absent diaphragm, bowel atresia and renal agenesis. Karyotypes have been reported as normal and no correlations with gender, parental age and teratogenic agents have been found. The principal theories are an extrinsic origin by early amniotic rupture, or a vascular origin due to an early vascular accident during embryological development. Single cases of familial occurrence have been documented. LBWC is fatal, with death occurring antenatally or early in the neonatal period. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core

3857641000052111 LBWC-komplex sv Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Sweden NRC maintained module (core metadata concept)

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Limb body wall complex (disorder)	Is a	Multiple malformation syndrome with limb defect as major feature	true	Inferred relationship	Some
Limb body wall complex (disorder)	Is a	medfödd anomali i bukväggen	false	Inferred relationship	Some
Limb body wall complex (disorder)	Associated morphology	utvecklingsabnormitet	false	Inferred relationship	Some	1
Limb body wall complex (disorder)	Occurrence	Congenital	true	Inferred relationship	Some	1
Limb body wall complex (disorder)	Finding site	bukvägg, struktur	false	Inferred relationship	Some	1
Limb body wall complex (disorder)	Associated morphology	Morphologically abnormal structure (morphologic abnormality)	true	Inferred relationship	Some	1
Limb body wall complex (disorder)	Pathological process (attribute)	Pathological developmental process	true	Inferred relationship	Some	1
Limb body wall complex (disorder)	Finding site	Structure of wall of abdominal proper segment of trunk	true	Inferred relationship	Some	1
Limb body wall complex (disorder)	Is a	Congenital anomaly of body wall	true	Inferred relationship	Some
Limb body wall complex (disorder)	Is a	Congenital anomaly of lower trunk	true	Inferred relationship	Some

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

This concept is not in any reference sets

Back to Start

Id	Description	Lang	Type	Status	Case?	Module
3304753015	Limb body wall complex (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
3304754014	Limb body wall complex	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
3304755010	LBWC (limb body wall complex) syndrome	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
3304756011	Limb body wall complex (LBWC) is a syndrome with features of severe multiple congenital anomalies. Clinical manifestations vary widely and include limb defects and visceral malformations, spinal abnormalities, absent diaphragm, bowel atresia and renal agenesis. Karyotypes have been reported as normal and no correlations with gender, parental age and teratogenic agents have been found. The principal theories are an extrinsic origin by early amniotic rupture, or a vascular origin due to an early vascular accident during embryological development. Single cases of familial occurrence have been documented. LBWC is fatal, with death occurring antenatally or early in the neonatal period.	en	Definition	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
3857641000052111	LBWC-komplex	sv	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Sweden NRC maintained module (core metadata concept)