233745009: Defect of diaphragm (disorder)

Status: retired, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Mar 2023. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

350249011 Defect of diaphragm en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

621971011 Defect of diaphragm (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

4988281000241117 défaut de diaphragme 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
défaut de diaphragme	Is a	Disorder of diaphragm (disorder)	false	Inferred relationship	Some
défaut de diaphragme	Finding site	Diaphragm structure	false	Inferred relationship	Some
défaut de diaphragme	Finding site	Entire body wall (body structure)	false	Inferred relationship	Some
défaut de diaphragme	Finding site	Body wall structure	false	Inferred relationship	Some
défaut de diaphragme	Is a	Lesion of soft tissue (disorder)	false	Inferred relationship	Some
défaut de diaphragme	Associated morphology	Defect	false	Inferred relationship	Some	1
défaut de diaphragme	Finding site	Diaphragm structure	false	Inferred relationship	Some	1
défaut de diaphragme	Is a	Lesion of skeletal muscle (disorder)	false	Inferred relationship	Some

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Congenital eventration of diaphragm	Is a	False	défaut de diaphragme	Inferred relationship	Some
Diaphragmatic hernia	Is a	False	défaut de diaphragme	Inferred relationship	Some
Congenital absence of diaphragm	Is a	False	défaut de diaphragme	Inferred relationship	Some
Aplasia of diaphragm (disorder)	Is a	False	défaut de diaphragme	Inferred relationship	Some
A rare genetic multiple congenital anomalies/dysmorphic syndrome characterized by diaphragmatic hernia, lung hypoplasia, ossification defect of the skull, and severe limb hypoplasia. Other clinical features may include, syndactyly, clinodactyly, extra spleen, absence of the femur or pelvic bone, partial intestinal malrotation, omphalocele and testicular atrophy.	Is a	False	défaut de diaphragme	Inferred relationship	Some

Reference Sets

Concept inactivation indicator reference set

POSSIBLY EQUIVALENT TO association reference set (foundation metadata concept)