725911008: Pierre Robin sequence, congenital heart defect, talipes syndrome (disorder)

• SNOMED CT Concept\Clinical finding\Disease\...
• \Genetic disease\Hereditary disease\...
• \Developmental hereditary disorder\Pierre Robin sequence, congenital heart defect, talipes syndrome
• \Sex-linked hereditary disorder\X-linked hereditary disease\X-linked recessive hereditary disease\Pierre Robin sequence, congenital heart defect, talipes syndrome
• \Congenital disease\Congenital malformation\Congenital malformation syndrome\Multiple system malformation syndrome\Pierre Robin sequence, congenital heart defect, talipes syndrome
• \Developmental disorder\Developmental hereditary disorder\Pierre Robin sequence, congenital heart defect, talipes syndrome
• \Developmental disorder\Congenital malformation\Congenital malformation syndrome\Multiple system malformation syndrome\Pierre Robin sequence, congenital heart defect, talipes syndrome

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2017. Module: SNOMED CT core module

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
3446379012	Pierre Robin sequence, congenital heart defect, talipes syndrome (disorder)	en	Fully specified name	Active	Entire term case sensitive	SNOMED CT core module
3446380010	TARP syndrome	en	Synonym	Active	Entire term case sensitive	SNOMED CT core module
3446381014	Pierre Robin sequence, congenital heart defect, talipes syndrome	en	Synonym	Active	Entire term case sensitive	SNOMED CT core module
3446382019	Pierre Robin syndrome, congenital heart defect, talipes syndrome	en	Synonym	Active	Entire term case sensitive	SNOMED CT core module
3446383012	TARP (talipes equinovarus, atrial septal defect, Robin sequence, persistence of left superior vena cava) syndrome	en	Synonym	Active	Entire term case sensitive	SNOMED CT core module

Expanded Value Set

This concept is not in any reference sets

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