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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
110661000077115 atrophie microvillositaire congénitale fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
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
382331000077111 atrophie microvillositaire congénitale (trouble) fr Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
624225011 Congenital microvillous atrophy (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core


1 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
atrophie microvillositaire congénitale Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
atrophie microvillositaire congénitale est un(e) (attribut) Congenital anomaly of small intestine (disorder) true Inferred relationship Some
atrophie microvillositaire congénitale est un(e) (attribut) Disorder of small intestine false Inferred relationship Some
atrophie microvillositaire congénitale est un(e) (attribut) Congenital disease false Inferred relationship Some
atrophie microvillositaire congénitale survenue (attribut) congénital false Inferred relationship Some
atrophie microvillositaire congénitale survenue (attribut) congénital true Inferred relationship Some 1
atrophie microvillositaire congénitale morphologie associée (attribut) Microvillus alteration true Inferred relationship Some 1
atrophie microvillositaire congénitale localisation d'une constatation (attribut) Structure of small intestine (body structure) true Inferred relationship Some 1
atrophie microvillositaire congénitale est un(e) (attribut) syndrome de malabsorption true Inferred relationship Some
atrophie microvillositaire congénitale localisation d'une constatation (attribut) Structure of small intestine (body structure) false Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group
Familial absence of villi est un(e) (attribut) True atrophie microvillositaire congénitale Inferred relationship Some

Reference Sets

Canada English language reference set (foundation metadata concept)

Description inactivation indicator reference set

GB English

US English

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