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783256001: Familial thrombomodulin anomalies (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2019. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
3758307019 Familial thrombomodulin anomalies (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
3758308012 Familial thrombomodulin anomalies en Synonym Active Entire term case insensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Familial thrombomodulin anomalies Is a Familial disease true Inferred relationship Existential restriction modifier
Familial thrombomodulin anomalies Is a Blood coagulation disorder true Inferred relationship Existential restriction modifier
Familial thrombomodulin anomalies Interprets Hemostatic function true Inferred relationship Existential restriction modifier 1
Familial thrombomodulin anomalies Has interpretation Abnormal true Inferred relationship Existential restriction modifier 1

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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