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439701000: Hereditary heparin cofactor II deficiency (disorder)


Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 30-Apr 2022. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
2788435014 Hereditary heparin cofactor II deficiency (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
2794143018 Hereditary heparin cofactor II deficiency en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3368241000052119 ärftlig brist på heparinkofaktor II sv Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Sweden NRC maintained module (core metadata concept)


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Hereditary heparin cofactor II deficiency (disorder) Is a Hereditary thrombophilia (disorder) true Inferred relationship Some
Hereditary heparin cofactor II deficiency (disorder) Is a Heparin cofactor II deficiency true Inferred relationship Some
Hereditary heparin cofactor II deficiency (disorder) Interprets Hemostatic function true Inferred relationship Some 1
Hereditary heparin cofactor II deficiency (disorder) Has interpretation Abnormal true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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