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95841006: hereditaire hypoplasminogenemie (aandoening)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
158737014 Hereditary hypoplasminogenemia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
512324012 Hereditary hypoplasminogenaemia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
840080012 Hereditary hypoplasminogenemia (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
6491041000146116 erfelijke hypoplasminogenemie nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
6491051000146118 hereditaire hypoplasminogenemie (aandoening) nl Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
6491061000146115 hereditaire hypoplasminogenemie nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)


1 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Hereditary hypoplasminogenemia Is a Hypoplasminogenaemia true Inferred relationship Some
Hereditary hypoplasminogenemia Is a Hereditary disorder of hematologic system false Inferred relationship Some
Hereditary hypoplasminogenemia Finding site Entire hematological system (body structure) false Inferred relationship Some
Hereditary hypoplasminogenemia Is a Hereditary disorder by system false Inferred relationship Some
Hereditary hypoplasminogenemia Finding site Body system structure false Inferred relationship Some
Hereditary hypoplasminogenemia Has definitional manifestation Hemostatic system finding false Inferred relationship Some
Hereditary hypoplasminogenemia Is a Hereditary disease true Inferred relationship Some
Hereditary hypoplasminogenemia Interprets Hemostatic function true Inferred relationship Some 1
Hereditary hypoplasminogenemia Has interpretation Abnormal true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group
Autosomal dominant deficiency of plasminogen Is a True Hereditary hypoplasminogenemia Inferred relationship Some

This concept is not in any reference sets

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