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439274008: Hereditary protein C deficiency (disorder)


Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 30-Apr 2022. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
2788412011 Hereditary protein C deficiency (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
2791269015 Hereditary protein C deficiency en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
2788412011 Hereditary protein C deficiency (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
2791269015 Hereditary protein C deficiency en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3389061001000112 Schwere hereditäre Thrombophilie durch kongenitalen Protein-C-Mangel de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5327621000241112 déficit en protéine C, héréditaire fr Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5327621000241112 déficit en protéine C, héréditaire fr Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3389061001000112 Schwere hereditäre Thrombophilie durch kongenitalen Protein-C-Mangel de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


3 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Hereditary protein C deficiency (disorder) Is a Protein C deficiency disease true Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary protein C deficiency (disorder) Is a Hereditary thrombophilia (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary protein C deficiency (disorder) Interprets Hemostatic function true Inferred relationship Existential restriction modifier (core metadata concept) 1
Hereditary protein C deficiency (disorder) Has interpretation Abnormal true Inferred relationship Existential restriction modifier (core metadata concept) 1

Inbound Relationships Type Active Source Characteristic Refinability Group
Heterozygous protein C deficiency (disorder) Is a True Hereditary protein C deficiency (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Homozygous protein C deficiency Is a True Hereditary protein C deficiency (disorder) Inferred relationship Existential restriction modifier (core metadata concept)

This concept is not in any reference sets

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