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235729009: Congenital microvillous atrophy (disorder)


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
353381016 Congenital microvillous atrophy en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
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 Only initial character case insensitive (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
3419301001000117 Mikrovillöse Einschluss-Krankheit de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
110661000077115 atrophie microvillositaire congénitale fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
110661000077115 atrophie microvillositaire congénitale fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3419301001000117 Mikrovillöse Einschluss-Krankheit de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


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 Existential restriction modifier (core metadata concept)
Congenital microvillous atrophy Finding site Structure of small intestine (body structure) false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital microvillous atrophy Is a Disorder of small intestine (disorder) false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital microvillous atrophy Is a Congenital disease false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital microvillous atrophy Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital microvillous atrophy Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital microvillous atrophy Associated morphology Microvillus alteration true Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital microvillous atrophy Finding site Structure of small intestine (body structure) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital microvillous atrophy Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital microvillous atrophy Is a Congenital anomaly of small intestine true Inferred relationship Existential restriction modifier (core metadata concept)

Inbound Relationships Type Active Source Characteristic Refinability Group
Familial absence of villi (disorder) Is a True Congenital microvillous atrophy Inferred relationship Existential restriction modifier (core metadata concept)

Reference Sets

Description inactivation indicator reference set

US English

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