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726708009: Familial isolated congenital asplenia (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2017. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3451940015 Familial isolated congenital asplenia (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3451941016 Familial isolated congenital asplenia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3451942011 A rare non-syndromic potentially life-threatening visceral malformation with 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. There is evidence this disorder is caused by heterozygous mutation in the RPSA gene on chromosome 3p21. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Familial isolated congenital asplenia (disorder) Is a Autosomal dominant hereditary disorder true Inferred relationship Some
Familial isolated congenital asplenia (disorder) Is a Congenital absence of spleen true Inferred relationship Some
Familial isolated congenital asplenia (disorder) Is a Familial disease true Inferred relationship Some
Familial isolated congenital asplenia (disorder) Is a Hereditary disorder by system true Inferred relationship Some
Familial isolated congenital asplenia (disorder) Associated morphology Congenital absence (morphologic abnormality) false Inferred relationship Some 1
Familial isolated congenital asplenia (disorder) Occurrence Congenital true Inferred relationship Some 1
Familial isolated congenital asplenia (disorder) Finding site Splenic structure true Inferred relationship Some 1
Familial isolated congenital asplenia (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Familial isolated congenital asplenia (disorder) Is a Asplenia (disorder) false Inferred relationship Some
Familial isolated congenital asplenia (disorder) Is a Aplasia of spleen (disorder) false Inferred relationship Some
Familial isolated congenital asplenia (disorder) Is a Developmental hereditary disorder true Inferred relationship Some
Familial isolated congenital asplenia (disorder) Associated morphology Absence (morphologic abnormality) true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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