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18604004: Factor XIII deficiency disease (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2007. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
31367019 Factor XIII deficiency disease en Synonym Active Only initial character case insensitive SNOMED CT core module
31368012 Factor XIII deficiency disease, NOS en Synonym Inactive Only initial character case insensitive SNOMED CT core module
31369016 Fibrin stabilizing factor deficiency en Synonym Active Entire term case insensitive SNOMED CT core module
478723018 Fibrin stabilising factor deficiency en Synonym Active Entire term case insensitive SNOMED CT core module
746118017 Factor XIII deficiency disease (disorder) en Fully specified name Active Only initial character case insensitive SNOMED CT core module
1222141018 Factor XIII deficiency en Synonym Active Only initial character case insensitive SNOMED CT core module

5 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Factor XIII deficiency disease Is a Hereditary coagulation factor deficiency false Inferred relationship Existential restriction modifier
Factor XIII deficiency disease Is a Fibrinogen abnormality false Inferred relationship Existential restriction modifier
Factor XIII deficiency disease Finding site Entire hematological system false Inferred relationship Existential restriction modifier
Factor XIII deficiency disease Interprets Nutritional deficiency false Inferred relationship Existential restriction modifier
Factor XIII deficiency disease Finding site Body system structure false Inferred relationship Existential restriction modifier
Factor XIII deficiency disease Has definitional manifestation Hemostatic system finding false Inferred relationship Existential restriction modifier
Factor XIII deficiency disease Is a Coagulation factor deficiency syndrome true Inferred relationship Existential restriction modifier
Factor XIII deficiency disease Interprets Hemostatic function true Inferred relationship Existential restriction modifier 1
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 deficiency disease Is a True Factor XIII deficiency disease Inferred relationship Existential restriction modifier
Acquired factor XIII deficiency disease Is a True Factor XIII deficiency disease Inferred relationship Existential restriction modifier
Hereditary factor I deficiency disease Is a False Factor XIII deficiency disease Inferred relationship Existential restriction modifier

This concept is not in any reference sets

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