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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
353383018 Familial absence of villi en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
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 Only initial character 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
5004821000241114 absence familliale des villosités fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5004821000241114 absence familliale des villosités fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Familial absence of villi (disorder) Is a Congenital anomaly of small intestine false Inferred relationship Existential restriction modifier (core metadata concept)
Familial absence of villi (disorder) Is a Congenital microvillous atrophy true Inferred relationship Existential restriction modifier (core metadata concept)
Familial absence of villi (disorder) Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept)
Familial absence of villi (disorder) Finding site Structure of small intestine (body structure) false Inferred relationship Existential restriction modifier (core metadata concept) 1
Familial absence of villi (disorder) Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept) 1
Familial absence of villi (disorder) Finding site Structure of digestive system (body structure) false Inferred relationship Existential restriction modifier (core metadata concept) 1
Familial absence of villi (disorder) Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept)
Familial absence of villi (disorder) Finding site Structure of small intestine (body structure) false Inferred relationship Existential restriction modifier (core metadata concept) 1
Familial absence of villi (disorder) Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept) 1
Familial absence of villi (disorder) Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 2
Familial absence of villi (disorder) Associated morphology anomalie du développement false Inferred relationship Existential restriction modifier (core metadata concept) 2
Familial absence of villi (disorder) Finding site Structure of small intestine (body structure) false Inferred relationship Existential restriction modifier (core metadata concept) 2
Familial absence of villi (disorder) Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 3
Familial absence of villi (disorder) Associated morphology Microvillus alteration false Inferred relationship Existential restriction modifier (core metadata concept) 3
Familial absence of villi (disorder) Finding site Structure of small intestine (body structure) false Inferred relationship Existential restriction modifier (core metadata concept) 3
Familial absence of villi (disorder) Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Familial absence of villi (disorder) Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
Familial absence of villi (disorder) Associated morphology Morphologically abnormal structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Familial absence of villi (disorder) Is a Disorder of gastrointestinal tract mucous membrane (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Familial absence of villi (disorder) Finding site Intestinal villus true Inferred relationship Existential restriction modifier (core metadata concept) 1
Familial absence of villi (disorder) Associated morphology Microvillus alteration true Inferred relationship Existential restriction modifier (core metadata concept) 1
Familial absence of villi (disorder) Is a Familial disease true Inferred relationship Existential restriction modifier (core metadata concept)
Familial absence of villi (disorder) Is a Disorder of soft tissue of trunk false Inferred relationship Existential restriction modifier (core metadata concept)
Familial absence of villi (disorder) Is a Disorder of soft tissue of abdominal cavity (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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