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439701000: Hereditary heparin cofactor II deficiency (disorder)


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

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 SNOMED CT core module
2794143018 Hereditary heparin cofactor II 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 heparin cofactor II deficiency Is a Hereditary thrombophilia true Inferred relationship Existential restriction modifier
Hereditary heparin cofactor II deficiency Is a Heparin cofactor II deficiency true Inferred relationship Existential restriction modifier
Hereditary heparin cofactor II deficiency Interprets Hemostatic function true Inferred relationship Existential restriction modifier 1
Hereditary heparin cofactor II deficiency Has interpretation Abnormal true Inferred relationship Existential restriction modifier 1

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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