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718689000: trisomie distale 10q (trouble)


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

Descriptions:

Id Description Lang Type Status Case? Module
1012791000172119 duplication distale 10q fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
3313220011 Distal trisomy 10q (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3313221010 Distal trisomy 10q en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3313227014 Distal duplication 10q en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
752481000241113 trisomie distale 10q (trouble) fr Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
942211000172118 trisomie distale 10q fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
3313228016 Distal trisomy of the long arm of chromosome 10 results in characteristics of pre and postnatal growth retardation, a pattern of specific facial features, hypotonia, and developmental and psychomotor delay. To date, approximately 40 cases have been reported. Most cases are diagnosed in infancy or in childhood. The range and severity of symptoms and physical findings may vary from case to case, depending upon the exact length and location of the duplicated portion of chromosome 10q. The duplicated region almost always includes 10qter, with the most frequent proximal breakpoint at 10q24 (with variation from q22 to q25). Interstitial duplications of 10q have also been reported. 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
Distal trisomy 10q (disorder) est un(e) (attribut) 10q partial trisomy syndrome true Inferred relationship Some
Distal trisomy 10q (disorder) morphologie associée (attribut) Partial trisomy true Inferred relationship Some 1
Distal trisomy 10q (disorder) survenue (attribut) congénital true Inferred relationship Some 1
Distal trisomy 10q (disorder) localisation d'une constatation (attribut) Chromosome pair 10 (cell structure) true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Canada English language reference set (foundation metadata concept)

GB English

US English

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