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235729009: Congenital microvillous atrophy (disorder)


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
353381016 Congenital microvillous atrophy en Synonym Active Entire term case insensitive SNOMED CT core module
353382011 Davidson disease en Synonym Active Entire term case sensitive SNOMED CT core module
624225011 Congenital microvillous atrophy (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core 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
Congenital microvillous atrophy Finding site Structure of small intestine false Inferred relationship Existential restriction modifier
Congenital microvillous atrophy Is a Disorder of small intestine false Inferred relationship Existential restriction modifier
Congenital microvillous atrophy Is a Congenital disease false Inferred relationship Existential restriction modifier
Congenital microvillous atrophy Occurrence Congenital false Inferred relationship Existential restriction modifier
Congenital microvillous atrophy Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Congenital microvillous atrophy Associated morphology Microvillus alteration true Inferred relationship Existential restriction modifier 1
Congenital microvillous atrophy Finding site Structure of small intestine true Inferred relationship Existential restriction modifier 1
Congenital microvillous atrophy Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Congenital microvillous atrophy Is a Congenital anomaly of small intestine true Inferred relationship Existential restriction modifier

Inbound Relationships Type Active Source Characteristic Refinability Group
Familial absence of villi Is a True Congenital microvillous atrophy Inferred relationship Existential restriction modifier

This concept is not in any reference sets

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