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441189007: Homozygous protein S 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
2789761017 Homozygous protein S deficiency (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
2795208016 Homozygous protein S deficiency en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Homozygous protein S deficiency (disorder) interprète (attribut) Hemostatic function (observable entity) true Inferred relationship Some 1
Homozygous protein S deficiency (disorder) a pour interprétation (attribut) anormal true Inferred relationship Some 1
Homozygous protein S deficiency (disorder) est un(e) (attribut) Hereditary protein S deficiency (disorder) true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Client's clinical problems, conditions, diagnoses, symptoms, findings, complaints reference set (foundation metadata concept)

Most commonly used clinical problems, conditions, diagnoses, symptoms, findings and complaints, as interpreted by the provider reference set (foundation metadata concept)

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