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439699000: Hereditary antithrombin III deficiency (disorder)


Status: current, Defined. Date: 28-Feb 2022. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
2788736011 Hereditary antithrombin III deficiency (disorder) en Fully specified name Active Initial character case insensitive SNOMED CT core
2791100010 Hereditary antithrombin III deficiency en Synonym Active Initial character case insensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Hereditary antithrombin III deficiency Interprets Haemostatic function true Inferred relationship Some 1
Hereditary antithrombin III deficiency Has interpretation Abnormal true Inferred relationship Some 1
Hereditary antithrombin III deficiency Is a Autosomal dominant hereditary disorder true Inferred relationship Some
Hereditary antithrombin III deficiency Interprets Measurement of antithrombin III activity in plasma true Inferred relationship Some 2
Hereditary antithrombin III deficiency Has interpretation Abnormally low true Inferred relationship Some 2
Hereditary antithrombin III deficiency Is a Hereditary thrombophilia true Inferred relationship Some
Hereditary antithrombin III deficiency Is a Antithrombin III deficiency true Inferred relationship Some

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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