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33169001: Factor XI deficiency, type II (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
55354017 Factor XI deficiency, type II en Synonym Active Only initial character case insensitive SNOMED CT core module
764538019 Factor XI deficiency, type II (disorder) en Fully specified name Active Only initial character case insensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Factor XI deficiency, type II Is a Hereditary factor XI deficiency disease true Inferred relationship Existential restriction modifier
Factor XI deficiency, type II Finding site Entire hematological system false Inferred relationship Existential restriction modifier
Factor XI deficiency, type II Finding site Body system structure false Inferred relationship Existential restriction modifier
Factor XI deficiency, type II Has definitional manifestation Hemostatic system finding false Inferred relationship Existential restriction modifier
Factor XI deficiency, type II Occurrence Congenital true Inferred relationship Existential restriction modifier 2
Factor XI deficiency, type II Interprets Hemostatic function true Inferred relationship Existential restriction modifier 1
Factor XI deficiency, type II Has interpretation Abnormal true Inferred relationship Existential restriction modifier 1

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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