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724356003: Hereditary combined deficiency of vitamin K-dependent clotting factors (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2017. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
3434469011 Hereditary combined deficiency of vitamin K-dependent clotting factors (disorder) en Fully specified name Active Only initial character case insensitive SNOMED CT core module
3434470012 Hereditary combined deficiency of vitamin K-dependent clotting factors en Synonym Active Only initial character case insensitive SNOMED CT core module
3434471011 Hereditary combined deficiency of factors II, VII, IX and X en Synonym Active Only initial character case insensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Hereditary combined deficiency of vitamin K-dependent clotting factors Is a Autosomal recessive hereditary disorder true Inferred relationship Existential restriction modifier
Hereditary combined deficiency of vitamin K-dependent clotting factors Is a Inborn error of metabolism true Inferred relationship Existential restriction modifier
Hereditary combined deficiency of vitamin K-dependent clotting factors Is a Hereditary combined coagulation factor deficiency true Inferred relationship Existential restriction modifier
Hereditary combined deficiency of vitamin K-dependent clotting factors Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Hereditary combined deficiency of vitamin K-dependent clotting factors Has interpretation Abnormal true Inferred relationship Existential restriction modifier 2
Hereditary combined deficiency of vitamin K-dependent clotting factors 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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