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1563006: Protein S deficiency disease (disorder)

Status: current, 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
3716018 Protein S deficiency disease en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
742491016 Protein S deficiency disease (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
1221214016 Protein S deficiency en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3716018 Protein S deficiency disease en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
742491016 Protein S deficiency disease (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
1221214016 Protein S deficiency en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
4391291000241116 déficit en protéine S fr Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
4391291000241116 déficit en protéine S fr Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

4 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Protein S deficiency disease Is a Deficiency of naturally occurring coagulation factor inhibitor true Inferred relationship Existential restriction modifier (core metadata concept)
Protein S deficiency disease Is a Thrombophilia true Inferred relationship Existential restriction modifier (core metadata concept)
Protein S deficiency disease Finding site Entire hematological system (body structure) false Inferred relationship Existential restriction modifier (core metadata concept)
Protein S deficiency disease Finding site Body system structure false Inferred relationship Existential restriction modifier (core metadata concept)
Protein S deficiency disease Has definitional manifestation Hemostatic system finding (finding) false Inferred relationship Existential restriction modifier (core metadata concept)
Protein S deficiency disease Interprets Hemostatic function true Inferred relationship Existential restriction modifier (core metadata concept) 1
Protein S deficiency disease Has interpretation Abnormal true Inferred relationship Existential restriction modifier (core metadata concept) 1
Inbound Relationships Type Active Source Characteristic Refinability Group
Hereditary protein S deficiency (disorder) Is a True Protein S deficiency disease Inferred relationship Existential restriction modifier (core metadata concept)
Protein-S-Mangel, erworbener Is a False Protein S deficiency disease Inferred relationship Existential restriction modifier (core metadata concept)
Family history of protein S deficiency (situation) Associated finding True Protein S deficiency disease Inferred relationship Existential restriction modifier (core metadata concept) 1
Protein-S-Mangel, erworbener Due to False Protein S deficiency disease Inferred relationship Existential restriction modifier (core metadata concept) 1
Acquired protein S deficiency Is a True Protein S deficiency disease Inferred relationship Existential restriction modifier (core metadata concept)

This concept is not in any reference sets

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