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439699000: Hereditary antithrombin III deficiency (disorder)


Status: current, Sufficiently defined by necessary conditions definition status. Date: 28-Feb 2022. Module: SNOMED CT core module

Descriptions:

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


0 descendants.

Expanded Value Set


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

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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