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439459008: Hereditary factor XIII B subunit deficiency (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
2789395015 Hereditary factor XIII B subunit deficiency (disorder) en Fully specified name Active Only initial character case insensitive SNOMED CT core module
2790347018 Hereditary factor XIII B subunit deficiency en Synonym Active Only initial character case insensitive SNOMED CT core module
2790348011 Hereditary factor XIII beta subunit deficiency en Synonym Active Only initial character case insensitive SNOMED CT core module
2790527013 Hereditary factor XIII type III 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 factor XIII B subunit deficiency Is a Hereditary factor XIII deficiency disease true Inferred relationship Existential restriction modifier
Hereditary factor XIII B subunit deficiency Interprets Hemostatic function true Inferred relationship Existential restriction modifier 1
Hereditary factor XIII B subunit 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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