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441188004: Homozygous protein C deficiency (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2009. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
2788436010 Homozygous protein C deficiency (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
2794654010 Homozygous protein C deficiency en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
2428341000052117 homozygot protein C-brist sv Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Sweden NRC maintained module (core metadata concept)


1 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Homozygous protein C deficiency (disorder) Is a Hereditary protein C deficiency (disorder) true Inferred relationship Some
Homozygous protein C deficiency (disorder) Interprets Hemostatic function true Inferred relationship Some 1
Homozygous protein C deficiency (disorder) Has interpretation Abnormal true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group
Neonatal purpura fulminans (homozygous protein C deficiency) (disorder) Is a True Homozygous protein C deficiency (disorder) Inferred relationship Some

This concept is not in any reference sets

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