FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.4-SNAPSHOT  |  FHIR Version n/a  User: [n/a]

76407009: Protein C 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
126889016 Protein C deficiency disease en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
817124014 Protein C deficiency disease (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
1233987014 Protein C deficiency en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
126889016 Protein C deficiency disease en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
817124014 Protein C deficiency disease (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
1233987014 Protein C deficiency en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
4639631000241116 maladie de déficit en protéine C fr Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
4639631000241116 maladie de déficit en protéine C fr Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

5 descendants. Search Descendants:

Expanded Value Set

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

This concept is not in any reference sets

Back to Start