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95840007: Hypoplasminogenemia (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
158735018 Hypoplasminogenemia en Synonym Active Entire term case insensitive SNOMED CT core module
512322011 Plasminogen deficiency en Synonym Active Entire term case insensitive SNOMED CT core module
512323018 Hypoplasminogenaemia en Synonym Active Entire term case insensitive SNOMED CT core module
840078018 Hypoplasminogenemia (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module

3 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Hypoplasminogenemia Is a Fibrinolytic bleeding syndrome true Inferred relationship Existential restriction modifier
Hypoplasminogenemia Is a Disorder involving the fibrinolytic system false Inferred relationship Existential restriction modifier
Hypoplasminogenemia Finding site Entire hematological system false Inferred relationship Existential restriction modifier
Hypoplasminogenemia Finding site Body system structure false Inferred relationship Existential restriction modifier
Hypoplasminogenemia Has definitional manifestation Hemostatic system finding false Inferred relationship Existential restriction modifier
Hypoplasminogenemia Interprets Hemostatic function true Inferred relationship Existential restriction modifier 1
Hypoplasminogenemia Has interpretation Abnormal true Inferred relationship Existential restriction modifier 1
Inbound Relationships Type Active Source Characteristic Refinability Group
Hereditary hypoplasminogenemia Is a True Hypoplasminogenemia Inferred relationship Existential restriction modifier
Acquired hypoplasminogenemia Is a True Hypoplasminogenemia Inferred relationship Existential restriction modifier

This concept is not in any reference sets

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