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235730004: Familial absence of villi (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
353383018 Familial absence of villi en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
624227015 Familial absence of villi (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Familial absence of villi Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Familial absence of villi survenue (attribut) congénital true Inferred relationship Some 1
Familial absence of villi morphologie associée (attribut) structure anormale sur le plan morphologique false Inferred relationship Some 1
Familial absence of villi est un(e) (attribut) Disorder of gastrointestinal tract mucous membrane (disorder) true Inferred relationship Some
Familial absence of villi localisation d'une constatation (attribut) Intestinal villus true Inferred relationship Some 1
Familial absence of villi morphologie associée (attribut) Microvillus alteration true Inferred relationship Some 1
Familial absence of villi est un(e) (attribut) Familial disease true Inferred relationship Some
Familial absence of villi est un(e) (attribut) affection des tissus mous du tronc true Inferred relationship Some
Familial absence of villi morphologie associée (attribut) Congenital anomaly false Inferred relationship Some 1
Familial absence of villi localisation d'une constatation (attribut) système digestif false Inferred relationship Some 1
Familial absence of villi survenue (attribut) congénital false Inferred relationship Some
Familial absence of villi localisation d'une constatation (attribut) Structure of small intestine (body structure) false Inferred relationship Some 1
Familial absence of villi morphologie associée (attribut) Congenital anomaly false Inferred relationship Some 1
Familial absence of villi survenue (attribut) congénital false Inferred relationship Some 2
Familial absence of villi morphologie associée (attribut) Developmental abnormality false Inferred relationship Some 2
Familial absence of villi localisation d'une constatation (attribut) Structure of small intestine (body structure) false Inferred relationship Some 2
Familial absence of villi survenue (attribut) congénital false Inferred relationship Some 3
Familial absence of villi morphologie associée (attribut) Microvillus alteration false Inferred relationship Some 3
Familial absence of villi localisation d'une constatation (attribut) Structure of small intestine (body structure) false Inferred relationship Some 3
Familial absence of villi est un(e) (attribut) Congenital anomaly of small intestine (disorder) false Inferred relationship Some
Familial absence of villi est un(e) (attribut) atrophie microvillositaire congénitale true Inferred relationship Some
Familial absence of villi survenue (attribut) congénital false Inferred relationship Some
Familial absence of villi localisation d'une constatation (attribut) Structure of small intestine (body structure) false Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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