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438372000: Hereditary factor IX deficiency disease with inhibitor (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2009. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
2787760013 Hereditary factor IX deficiency disease with inhibitor (disorder) en Fully specified name Active Only initial character case insensitive SNOMED CT core module
2791040019 Haemophilia B with inhibitor en Synonym Active Only initial character case insensitive SNOMED CT core module
2791041015 Hemophilia B with inhibitor en Synonym Active Only initial character case insensitive SNOMED CT core module
2791042010 Hereditary factor IX deficiency disease with inhibitor en Synonym Active Only initial character case insensitive SNOMED CT core module


3 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Hereditary factor IX deficiency disease with inhibitor Is a Hereditary factor IX deficiency disease true Inferred relationship Existential restriction modifier
Hereditary factor IX deficiency disease with inhibitor Occurrence Congenital true Inferred relationship Existential restriction modifier 2
Hereditary factor IX deficiency disease with inhibitor Interprets Hemostatic function true Inferred relationship Existential restriction modifier 1
Hereditary factor IX deficiency disease with inhibitor Has interpretation Abnormal true Inferred relationship Existential restriction modifier 1

Inbound Relationships Type Active Source Characteristic Refinability Group
Severe hereditary factor IX deficiency disease with inhibitor Is a True Hereditary factor IX deficiency disease with inhibitor Inferred relationship Existential restriction modifier
Mild hereditary factor IX deficiency disease with inhibitor Is a True Hereditary factor IX deficiency disease with inhibitor Inferred relationship Existential restriction modifier
Moderate hereditary factor IX deficiency disease with inhibitor Is a True Hereditary factor IX deficiency disease with inhibitor Inferred relationship Existential restriction modifier

This concept is not in any reference sets

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