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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


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Hereditary heparin cofactor II deficiency (disorder) interprète (attribut) Hemostatic function (observable entity) true Inferred relationship Some 1
Hereditary heparin cofactor II deficiency (disorder) a pour interprétation (attribut) anormal true Inferred relationship Some 1
Hereditary heparin cofactor II deficiency (disorder) est un(e) (attribut) Hereditary thrombophilia (disorder) true Inferred relationship Some
Hereditary heparin cofactor II deficiency (disorder) est un(e) (attribut) Heparin cofactor II deficiency true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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