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

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

Status: retired, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module Reference Sets
243588017 (Fetus with hereditary disease) or (cystic fibrosis in pregnancy) en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core Description inactivation indicator reference set: Concept non-current
2755232016 (Fetus with hereditary disease) or (cystic fibrosis in pregnancy) (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core Description inactivation indicator reference set: Concept non-current

0 descendants.

Expanded Value Set


Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Concept inactivation indicator reference set

SAME AS association reference set (foundation metadata concept)

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