707147002: Asplenia (disorder)

SNOMED CT Concept\Clinical finding (finding)\...

\Viscus structure finding (finding)\Abdominal organ finding\Disorder of spleen\Congenital or functional absence of spleen

\Finding of trunk structure (finding)\Finding of abdominopelvic segment of trunk (finding)\Disorder of abdominopelvic segment of trunk\Disorder of abdomen (disorder)\Disorder of spleen\Congenital or functional absence of spleen
\Finding of trunk structure (finding)\Finding of abdominopelvic segment of trunk (finding)\Finding of abdomen\Abdominal organ finding\Disorder of spleen\Congenital or functional absence of spleen
\Finding of trunk structure (finding)\Finding of abdominopelvic segment of trunk (finding)\Finding of abdomen\Disorder of abdomen (disorder)\Disorder of spleen\Congenital or functional absence of spleen
\Finding of trunk structure (finding)\Disorder of trunk (disorder)\Disorder of abdominopelvic segment of trunk\Disorder of abdomen (disorder)\Disorder of spleen\Congenital or functional absence of spleen

\Disease\Disorder of body system\Disorder of immune structure (disorder)\Disorder of lymphoid system (disorder)\Disorder of spleen\Congenital or functional absence of spleen
\Disease\Disorder of body system\Disorder of hematopoietic structure (disorder)\Disorder of lymphoid system (disorder)\Disorder of spleen\Congenital or functional absence of spleen
\Disease\Disorder of trunk (disorder)\Disorder of abdominopelvic segment of trunk\Disorder of abdomen (disorder)\Disorder of spleen\Congenital or functional absence of spleen

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2015. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

3028913010 Congenital or functional absence of spleen en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core

3028873019 Asplenia (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

3028874013 Asplenia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Congenital or functional absence of spleen	Is a	Disorder of spleen	true	Inferred relationship	Some
Congenital or functional absence of spleen	Finding site	Splenic structure	true	Inferred relationship	Some	1

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Functional asplenia	Is a	True	Congenital or functional absence of spleen	Inferred relationship	Some
Congenital absence of spleen	Is a	True	Congenital or functional absence of spleen	Inferred relationship	Some
Thrombocytopathy, asplenia and miosis (disorder)	Is a	True	Congenital or functional absence of spleen	Inferred relationship	Some
Asplenia following surgical procedure (disorder)	Is a	True	Congenital or functional absence of spleen	Inferred relationship	Some
Familial isolated congenital asplenia is a rare, non-syndromic, potentially life-threatening visceral malformation characterised by the absence of normal spleen function, resulting in a primary immunodeficiency. Typically, the condition manifests with severe, recurrent, overwhelming infections (especially pneumococcal sepsis) in otherwise apparently healthy infants. In adults with no history of severe sepsis in infancy, thrombocytosis may be the presenting sign. Howell-Jolly bodies on blood smears and an absent spleen on abdominal ultrasound examination are highly suggestive associated findings.	Is a	False	Congenital or functional absence of spleen	Inferred relationship	Some
Ivemarks syndom	Is a	False	Congenital or functional absence of spleen	Inferred relationship	Some

Reference Sets

Description inactivation indicator reference set