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235729009: congenitale microvillusatrofie (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
353381016 Congenital microvillous atrophy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
353382011 Davidson disease en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
624225011 Congenital microvillous atrophy (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
9041381000146118 congenitale microvillusatrofie (aandoening) nl Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
9041391000146116 congenitale microvillusatrofie nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
9941171000146110 aangeboren microvillusatrofie 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
Congenital microvillous atrophy Is a Malabsorption syndrome true Inferred relationship Some
Congenital microvillous atrophy Finding site Structure of small intestine (body structure) false Inferred relationship Some
Congenital microvillous atrophy Is a Disorder of small intestine false Inferred relationship Some
Congenital microvillous atrophy Is a Congenital disease (disorder) false Inferred relationship Some
Congenital microvillous atrophy Occurrence Congenital false Inferred relationship Some
Congenital microvillous atrophy Occurrence Congenital true Inferred relationship Some 1
Congenital microvillous atrophy Associated morphology Microvillus alteration true Inferred relationship Some 1
Congenital microvillous atrophy Finding site Structure of small intestine (body structure) true Inferred relationship Some 1
Congenital microvillous atrophy Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Congenital microvillous atrophy Is a Congenital anomaly of small intestine true Inferred relationship Some
Congenital microvillous atrophy Is a Congenital disorder of intestine (disorder) false Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group
Familial absence of villi Is a True Congenital microvillous atrophy Inferred relationship Some

Reference Sets

Description inactivation indicator reference set

US English

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