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702624008: Aplasia of spleen (disorder)


Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2014. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3005254019 Aplasia of spleen (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3005263017 Aplasia of spleen en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3005336016 Splenic aplasia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5785641000241118 aplasie de la rate fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5785651000241115 aplasie splénique fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


1 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Aplasia of spleen (disorder) Is a Congenital anomaly of spleen true Inferred relationship Some
Aplasia of spleen (disorder) Occurrence Congenital true Inferred relationship Some 1
Aplasia of spleen (disorder) Associated morphology Aplasia true Inferred relationship Some 1
Aplasia of spleen (disorder) Finding site Splenic structure true Inferred relationship Some 1
Aplasia of spleen (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group
Congenital absence of spleen Is a False Aplasia of spleen (disorder) 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 Aplasia of spleen (disorder) Inferred relationship Some
Bilateral right-sidedness sequence Is a False Aplasia of spleen (disorder) Inferred relationship Some
Agenesis of spleen Is a True Aplasia of spleen (disorder) Inferred relationship Some

This concept is not in any reference sets

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