156177002: (Fetus with hereditary disease) or (cystic fibrosis in pregnancy) (disorder)

• (Fetus with hereditary disease) or (cystic fibrosis in pregnancy)

Status: retired, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
243588017	(Fetus with hereditary disease) or (cystic fibrosis in pregnancy)	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
2755232016	(Fetus with hereditary disease) or (cystic fibrosis in pregnancy) (disorder)	en	Fully specified name	Active	Initial character case insensitive	SNOMED CT core

Expanded Value Set

Reference Sets

Concept inactivation indicator reference set

SAME AS association reference set

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