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439699000: Hereditary antithrombin III deficiency (disorder)


Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). 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 Only initial character case insensitive (core metadata concept) SNOMED CT core
2791100010 Hereditary antithrombin III deficiency en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
5900601000172111 déficit en antithrombine III, héréditaire fr Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) Belgian module (core metadata concept)
11247361000172111 déficit héréditaire en antithrombine III fr Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) Belgian module (core metadata concept)
11247371000172119 déficit héréditaire en AT III fr Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) Belgian module (core metadata concept)
11247381000172116 thrombophilie héréditaire due au déficit congénital en antithrombine 3 fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Belgian module (core metadata concept)
5153061000172118 hereditaire antitrombine III-deficiëntie nl Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) Belgian module (core metadata concept)


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Hereditary antithrombin III deficiency (disorder) Is a Hereditary thrombophilia (disorder) true Inferred relationship Some
Hereditary antithrombin III deficiency (disorder) Is a Antithrombin III deficiency true Inferred relationship Some
Hereditary antithrombin III deficiency (disorder) Interprets Hemostatic function true Inferred relationship Some 1
Hereditary antithrombin III deficiency (disorder) Has interpretation Abnormal true Inferred relationship Some 1
Hereditary antithrombin III deficiency (disorder) Is a Autosomal dominant hereditary disorder true Inferred relationship Some
Hereditary antithrombin III deficiency (disorder) Interprets Plasma antithrombin III activity true Inferred relationship Some 2
Hereditary antithrombin III deficiency (disorder) Has interpretation Abnormally low (qualifier value) true Inferred relationship Some 2

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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