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50189006: Hereditary factor XIII deficiency disease (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2002. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
83596013 Hereditary factor XIII deficiency disease en Synonym Active Only initial character case insensitive SNOMED CT core module
83597016 Laki-Lorand factor deficiency disease en Synonym Active Entire term case sensitive SNOMED CT core module
787949018 Hereditary factor XIII deficiency disease (disorder) en Fully specified name 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 XIII deficiency disease Is a Factor XIII deficiency disease true Inferred relationship Existential restriction modifier
Hereditary factor XIII deficiency disease Interprets Nutritional deficiency false Inferred relationship Existential restriction modifier
Hereditary factor XIII deficiency disease Finding site Entire hematological system false Inferred relationship Existential restriction modifier
Hereditary factor XIII deficiency disease Finding site Body system structure false Inferred relationship Existential restriction modifier
Hereditary factor XIII deficiency disease Has definitional manifestation Hemostatic system finding false Inferred relationship Existential restriction modifier
Hereditary factor XIII deficiency disease Is a Hereditary coagulation factor deficiency true Inferred relationship Existential restriction modifier
Hereditary factor XIII deficiency disease Interprets Hemostatic function true Inferred relationship Existential restriction modifier 1
Hereditary factor XIII deficiency disease Has interpretation Abnormal true Inferred relationship Existential restriction modifier 1
Inbound Relationships Type Active Source Characteristic Refinability Group
Hereditary factor XIII A subunit and B subunit deficiency Is a True Hereditary factor XIII deficiency disease Inferred relationship Existential restriction modifier
Hereditary factor XIII B subunit deficiency Is a True Hereditary factor XIII deficiency disease Inferred relationship Existential restriction modifier
Hereditary factor XIII A subunit deficiency Is a True Hereditary factor XIII deficiency disease Inferred relationship Existential restriction modifier

This concept is not in any reference sets

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