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438827002: Hereditary thrombophilic dysfibrinogenemia (disorder)


Status: current, Defined. Date: 30-Apr 2022. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
2786839018 Hereditary thrombophilic dysfibrinogenemia (disorder) en Fully specified name Active Case insensitive SNOMED CT core
2792833017 Hereditary thrombophilic dysfibrinogenaemia en Synonym Active Case insensitive SNOMED CT core
2794775012 Hereditary thrombophilic dysfibrinogenemia en Synonym Active Case insensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Hereditary thrombophilic dysfibrinogenemia Interprets Haemostatic function true Inferred relationship Some 1
Hereditary thrombophilic dysfibrinogenemia Has interpretation Abnormal true Inferred relationship Some 1
Hereditary thrombophilic dysfibrinogenemia Is a Hereditary thrombophilia true Inferred relationship Some
Hereditary thrombophilic dysfibrinogenemia Is a Hereditary dysfibrinogenaemia true Inferred relationship Some
Hereditary thrombophilic dysfibrinogenemia Occurrence Congenital true Inferred relationship Some 2

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

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