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439145006: Congenital hypofibrinogenemia (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
2789363016 Congenital hypofibrinogenemia (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
2794588013 Congenital hypofibrinogenemia en Synonym Active Entire term case insensitive SNOMED CT core module
2794589017 Congenital hypofibrinogenaemia en Synonym Active Entire term case insensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Congenital hypofibrinogenemia Is a Hereditary factor I deficiency disease true Inferred relationship Existential restriction modifier
Congenital hypofibrinogenemia Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Congenital hypofibrinogenemia Has interpretation Abnormal true Inferred relationship Existential restriction modifier 2
Congenital hypofibrinogenemia Interprets Hemostatic function true Inferred relationship Existential restriction modifier 2

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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