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234441009: Carrier of hereditary factor VIII deficiency disease (finding)

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
351261012 Hemophilia A carrier en Synonym Active Only initial character case insensitive SNOMED CT core module
351262017 Haemophilia A carrier en Synonym Active Only initial character case insensitive SNOMED CT core module
2789302011 Carrier of hereditary factor VIII deficiency disease (finding) en Fully specified name Active Only initial character case insensitive SNOMED CT core module
2791271015 Carrier of hereditary factor VIII deficiency disease en Synonym Active Only initial character case insensitive SNOMED CT core module

1 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Carrier of hereditary factor VIII deficiency disease Is a Hemophilia carrier true Inferred relationship Existential restriction modifier
Carrier of hereditary factor VIII deficiency disease Is a Hereditary factor VIII deficiency disease false Inferred relationship Existential restriction modifier
Carrier of hereditary factor VIII deficiency disease Finding site Entire hematological system false Inferred relationship Existential restriction modifier
Carrier of hereditary factor VIII deficiency disease Finding site Body system structure false Inferred relationship Existential restriction modifier
Carrier of hereditary factor VIII deficiency disease Has definitional manifestation Hemostatic system finding false Inferred relationship Existential restriction modifier
Carrier of hereditary factor VIII deficiency disease Interprets General clinical state true Inferred relationship Existential restriction modifier 1
Inbound Relationships Type Active Source Characteristic Refinability Group
Asymptomatic carrier of hereditary factor VIII deficiency disease Is a True Carrier of hereditary factor VIII deficiency disease Inferred relationship Existential restriction modifier

This concept is not in any reference sets

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