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234458004: Hypodysfibrinogenemia (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
351287012 Hypodysfibrinogenaemia en Synonym Active Entire term case insensitive SNOMED CT core module
351288019 Hypodysfibrinogenemia en Synonym Active Entire term case insensitive SNOMED CT core module
622781017 Hypodysfibrinogenemia (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module

0 descendants.

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Hypodysfibrinogenemia Is a Congenital fibrinogen abnormality true Inferred relationship Existential restriction modifier
Hypodysfibrinogenemia Finding site Entire hematological system false Inferred relationship Existential restriction modifier
Hypodysfibrinogenemia Occurrence Congenital true Inferred relationship Existential restriction modifier 2
Hypodysfibrinogenemia Finding site Body system structure false Inferred relationship Existential restriction modifier
Hypodysfibrinogenemia Has definitional manifestation Hemostatic system finding false Inferred relationship Existential restriction modifier
Hypodysfibrinogenemia Interprets Hemostatic function true Inferred relationship Existential restriction modifier 1
Hypodysfibrinogenemia Has interpretation Abnormal true Inferred relationship Existential restriction modifier 1
Hypodysfibrinogenemia Is a Autosomal hereditary disorder true Inferred relationship Existential restriction modifier
Hypodysfibrinogenemia Is a Fibrinogen deficiency true Inferred relationship Existential restriction modifier
Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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