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722430008: Distal trisomy 6p syndrome (disorder)


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
3332034019 Distal duplication 6p en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3332035018 Telomeric duplication 6p en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3332036017 Distal trisomy 6p syndrome (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3332037014 Distal trisomy 6p syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5402921019 Distal trisomy of the short arm of chromosome 6 is characterized by pre- and postnatal growth retardation, a pattern of specific facial features (mostly of the eyes), microcephaly, and developmental delay. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5402922014 Distal trisomy of the short arm of chromosome 6 is characterised by pre- and postnatal growth retardation, a pattern of specific facial features (mostly of the eyes), microcephaly, and developmental delay. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3332034019 Distal duplication 6p en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3332034019 Distal duplication 6p en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3332035018 Telomeric duplication 6p en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3332035018 Telomeric duplication 6p en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3332036017 Distal trisomy 6p syndrome (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3332036017 Distal trisomy 6p syndrome (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3332037014 Distal trisomy 6p syndrome en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3332037014 Distal trisomy 6p syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3332038016 Distal trisomy of the short arm of chromosome 6 has characteristics of pre and postnatal growth retardation, a pattern of specific facial features (mostly of the eyes), microcephaly, and developmental delay. The duplicated region almost always includes 6pter, with proximal breakpoints ranging from 6p21 to 6p25. Interstitial duplications of 6p have also been reported with different phenotypes depending on their size and location. Most cases of distal trisomy 6p result from missegregation of a familial balanced translocation, or pericentric inversion, and are accompanied by another chromosomal imbalance. Intrachromosomal duplications or de novo translocations are also observed. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5402921019 Distal trisomy of the short arm of chromosome 6 is characterized by pre- and postnatal growth retardation, a pattern of specific facial features (mostly of the eyes), microcephaly, and developmental delay. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5402922014 Distal trisomy of the short arm of chromosome 6 is characterised by pre- and postnatal growth retardation, a pattern of specific facial features (mostly of the eyes), microcephaly, and developmental delay. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3454171001000116 Trisomie 6p, distale de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5483921000241112 trisomie distale 6p fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5483921000241112 trisomie distale 6p fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3454171001000116 Trisomie 6p, distale de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Distal trisomy 6p syndrome (disorder) Is a Anomaly of chromosome pair 6 false Inferred relationship Existential restriction modifier (core metadata concept)
Distal trisomy 6p syndrome (disorder) Is a Trisomy and partial trisomy of autosome false Inferred relationship Existential restriction modifier (core metadata concept)
Distal trisomy 6p syndrome (disorder) Associated morphology Partial trisomy true Inferred relationship Existential restriction modifier (core metadata concept) 1
Distal trisomy 6p syndrome (disorder) Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
Distal trisomy 6p syndrome (disorder) Finding site Chromosome pair 6 (cell structure) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Distal trisomy 6p syndrome (disorder) Is a Partial trisomy of chromosome 6 (disorder) false Inferred relationship Existential restriction modifier (core metadata concept)
Distal trisomy 6p syndrome (disorder) Is a 6p partial trisomy syndrome true Inferred relationship Existential restriction modifier (core metadata concept)

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Component annotation with string value reference set (foundation metadata concept)

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