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439459008: Hereditary factor XIII B subunit deficiency (disorder)


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

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 (core metadata concept) SNOMED CT core
2790347018 Hereditary factor XIII B subunit deficiency en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
2790348011 Hereditary factor XIII beta subunit deficiency en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
2790527013 Hereditary factor XIII type III 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 factor XIII B subunit deficiency (disorder) interprète (attribut) Hemostatic function (observable entity) true Inferred relationship Some 1
Hereditary factor XIII B subunit deficiency (disorder) a pour interprétation (attribut) anormal true Inferred relationship Some 1
Hereditary factor XIII B subunit deficiency (disorder) est un(e) (attribut) Hereditary factor XIII deficiency disease (disorder) true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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