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1197428008: Combined immunodeficiency, enteropathy spectrum (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 28-Feb 2022. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
4696302016 CID-MIA/early-onset IBD - combined immunodeficiency-multiple intestinal atresia/early-onset inflammatory bowel disease en Synonym Active Entire term case sensitive SNOMED CT core module
4696305019 Combined immunodeficiency, enteropathy spectrum en Synonym Active Entire term case insensitive SNOMED CT core module
4696306018 Combined immunodeficiency, enteropathy spectrum (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Combined immunodeficiency, enteropathy spectrum Is a Inflammation of intestine true Inferred relationship Existential restriction modifier
Combined immunodeficiency, enteropathy spectrum Is a Inflammatory bowel disease true Inferred relationship Existential restriction modifier
Combined immunodeficiency, enteropathy spectrum Is a Congenital immunodeficiency disease true Inferred relationship Existential restriction modifier
Combined immunodeficiency, enteropathy spectrum Is a Developmental hereditary disorder true Inferred relationship Existential restriction modifier
Combined immunodeficiency, enteropathy spectrum Is a Digestive system hereditary disorder true Inferred relationship Existential restriction modifier
Combined immunodeficiency, enteropathy spectrum Is a Combined immunodeficiency disease true Inferred relationship Existential restriction modifier
Combined immunodeficiency, enteropathy spectrum Is a Autosomal recessive hereditary disorder true Inferred relationship Existential restriction modifier
Combined immunodeficiency, enteropathy spectrum Is a Congenital atresia of intestinal tract true Inferred relationship Existential restriction modifier
Combined immunodeficiency, enteropathy spectrum Occurrence Congenital true Inferred relationship Existential restriction modifier 2
Combined immunodeficiency, enteropathy spectrum Finding site Intestinal structure true Inferred relationship Existential restriction modifier 2
Combined immunodeficiency, enteropathy spectrum Associated morphology Congenital atresia true Inferred relationship Existential restriction modifier 2
Combined immunodeficiency, enteropathy spectrum Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 2
Combined immunodeficiency, enteropathy spectrum Finding site Intestinal structure true Inferred relationship Existential restriction modifier 1
Combined immunodeficiency, enteropathy spectrum Associated morphology Inflammatory morphology true Inferred relationship Existential restriction modifier 1
Combined immunodeficiency, enteropathy spectrum Pathological process Dysregulated host response true Inferred relationship Existential restriction modifier 1
Combined immunodeficiency, enteropathy spectrum Is a Hereditary white blood cell disorder true Inferred relationship Existential restriction modifier
Combined immunodeficiency, enteropathy spectrum Is a Lymphocytopenia true Inferred relationship Existential restriction modifier
Combined immunodeficiency, enteropathy spectrum Interprets Lymphocyte count true Inferred relationship Existential restriction modifier 3
Combined immunodeficiency, enteropathy spectrum Has interpretation Below reference range true Inferred relationship Existential restriction modifier 3

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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