235730004: Familial absence of villi (disorder)

SNOMED CT Concept\Clinical finding\...

\Skin AND/OR mucosa finding\Mucosal finding\Disorder of mucous membrane\Disorder of gastrointestinal tract mucous membrane\Familial absence of villi

\Viscus structure finding\Abdominal organ finding\Bowel finding\...

\Finding of small intestine\Disorder of small intestine\Congenital anomaly of small intestine\Congenital microvillous atrophy\Familial absence of villi

\Disorder of intestine\Congenital anomaly of intestinal tract\Congenital anomaly of small intestine\Congenital microvillous atrophy\Familial absence of villi
\Disorder of intestine\Disorder of small intestine\Congenital anomaly of small intestine\Congenital microvillous atrophy\Familial absence of villi

\General finding of soft tissue\Disorder of soft tissue\Disorder of soft tissue of trunk\Familial absence of villi

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2002. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module

353383018 Familial absence of villi en Synonym Active Entire term case insensitive SNOMED CT core module

624227015 Familial absence of villi (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Familial absence of villi	Is a	Congenital anomaly of small intestine	false	Inferred relationship	Existential restriction modifier
Familial absence of villi	Is a	Congenital microvillous atrophy	true	Inferred relationship	Existential restriction modifier
Familial absence of villi	Occurrence	Congenital	false	Inferred relationship	Existential restriction modifier
Familial absence of villi	Finding site	Structure of small intestine	false	Inferred relationship	Existential restriction modifier	1
Familial absence of villi	Associated morphology	Congenital anomaly	false	Inferred relationship	Existential restriction modifier	1
Familial absence of villi	Finding site	Structure of digestive system	false	Inferred relationship	Existential restriction modifier	1
Familial absence of villi	Occurrence	Congenital	false	Inferred relationship	Existential restriction modifier
Familial absence of villi	Finding site	Structure of small intestine	false	Inferred relationship	Existential restriction modifier	1
Familial absence of villi	Associated morphology	Congenital anomaly	false	Inferred relationship	Existential restriction modifier	1
Familial absence of villi	Occurrence	Congenital	false	Inferred relationship	Existential restriction modifier	2
Familial absence of villi	Associated morphology	Developmental anomaly	false	Inferred relationship	Existential restriction modifier	2
Familial absence of villi	Finding site	Structure of small intestine	false	Inferred relationship	Existential restriction modifier	2
Familial absence of villi	Occurrence	Congenital	false	Inferred relationship	Existential restriction modifier	3
Familial absence of villi	Associated morphology	Microvillus alteration	false	Inferred relationship	Existential restriction modifier	3
Familial absence of villi	Finding site	Structure of small intestine	false	Inferred relationship	Existential restriction modifier	3
Familial absence of villi	Pathological process	Pathological developmental process	true	Inferred relationship	Existential restriction modifier	1
Familial absence of villi	Occurrence	Congenital	true	Inferred relationship	Existential restriction modifier	1
Familial absence of villi	Associated morphology	Morphologically abnormal structure	false	Inferred relationship	Existential restriction modifier	1
Familial absence of villi	Is a	Disorder of gastrointestinal tract mucous membrane	true	Inferred relationship	Existential restriction modifier
Familial absence of villi	Finding site	Structure of intestinal villus	true	Inferred relationship	Existential restriction modifier	1
Familial absence of villi	Associated morphology	Microvillus alteration	true	Inferred relationship	Existential restriction modifier	1
Familial absence of villi	Is a	Familial disease	true	Inferred relationship	Existential restriction modifier
Familial absence of villi	Is a	Disorder of soft tissue of trunk	true	Inferred relationship	Existential restriction modifier

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

This concept is not in any reference sets

Back to Start

Id	Description	Lang	Type	Status	Case?	Module
353383018	Familial absence of villi	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
624227015	Familial absence of villi (disorder)	en	Fully specified name	Active	Entire term case insensitive	SNOMED CT core module