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72837006: Sex chromosome X (cell structure)

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
1204482016 Sex chromosome X (cell structure) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
120982015 Sex chromosome X en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

0 descendants.

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Sex chromosome X (cell structure) est un(e) (attribut) Sex chromosome (cell structure) true Inferred relationship Some
Sex chromosome X (cell structure) partie de Nucleus (cell structure) false Additional relationship Some
Inbound Relationships Type Active Source Characteristic Refinability Group
Chromosome Xp11.3 microdeletion syndrome (disorder) localisation d'une constatation (attribut) False Sex chromosome X (cell structure) Inferred relationship Some 3
Chromosome Xq28 trisomy (disorder) localisation d'une constatation (attribut) True Sex chromosome X (cell structure) Inferred relationship Some 2
Alport syndrome, intellectual disability, midface hypoplasia, elliptocytosis syndrome (disorder) localisation d'une constatation (attribut) False Sex chromosome X (cell structure) Inferred relationship Some 5
Microduplication Xp11.22p11.23 syndrome (disorder) localisation d'une constatation (attribut) False Sex chromosome X (cell structure) Inferred relationship Some 1
X-linked diffuse leiomyomatosis with Alport syndrome (disorder) localisation d'une constatation (attribut) True Sex chromosome X (cell structure) Inferred relationship Some 4
Chromosome Xp22.3 microdeletion syndrome (disorder) localisation d'une constatation (attribut) True Sex chromosome X (cell structure) Inferred relationship Some 2
Chromosome Xp22.3 microdeletion syndrome (disorder) localisation d'une constatation (attribut) False Sex chromosome X (cell structure) Inferred relationship Some 3
Atypical Norrie disease due to monosomy Xp11.3 (disorder) localisation d'une constatation (attribut) True Sex chromosome X (cell structure) Inferred relationship Some 2
Atypical Norrie disease due to monosomy Xp11.3 (disorder) localisation d'une constatation (attribut) False Sex chromosome X (cell structure) Inferred relationship Some 3
Klinefelter syndrome localisation d'une constatation (attribut) False Sex chromosome X (cell structure) Inferred relationship Some
Trisomy X syndrome localisation d'une constatation (attribut) True Sex chromosome X (cell structure) Inferred relationship Some 1
syndrome de Turner localisation d'une constatation (attribut) False Sex chromosome X (cell structure) Inferred relationship Some 1
XXXXY syndrome localisation d'une constatation (attribut) False Sex chromosome X (cell structure) Inferred relationship Some 1
Penta X syndrome localisation d'une constatation (attribut) False Sex chromosome X (cell structure) Inferred relationship Some 1
XX males localisation d'une constatation (attribut) False Sex chromosome X (cell structure) Inferred relationship Some 1
XXXY syndrome localisation d'une constatation (attribut) False Sex chromosome X (cell structure) Inferred relationship Some 1
Mixed gonadal dysgenesis localisation d'une constatation (attribut) False Sex chromosome X (cell structure) Inferred relationship Some 3
syndrome de duplication Xq12-q13.3 localisation d'une constatation (attribut) False Sex chromosome X (cell structure) Inferred relationship Some 1
X small rings localisation d'une constatation (attribut) True Sex chromosome X (cell structure) Inferred relationship Some 1
X-linked acrogigantism localisation d'une constatation (attribut) False Sex chromosome X (cell structure) Inferred relationship Some 2
49,XXXYY syndrome localisation d'une constatation (attribut) False Sex chromosome X (cell structure) Inferred relationship Some 1
Turner's phenotype, karyotype normal localisation d'une constatation (attribut) False Sex chromosome X (cell structure) Inferred relationship Some 1
Turner's phenotype, mosaicism 45, X; 46, XX or 45, X; 46, XY localisation d'une constatation (attribut) False Sex chromosome X (cell structure) Inferred relationship Some 1
Klinefelter's syndrome, XXYY localisation d'une constatation (attribut) False Sex chromosome X (cell structure) Inferred relationship Some 1
Klinefelter's syndrome, XY/XXY mosaic localisation d'une constatation (attribut) False Sex chromosome X (cell structure) Inferred relationship Some 1
Turner's phenotype, partial X deletion karyotype localisation d'une constatation (attribut) False Sex chromosome X (cell structure) Inferred relationship Some 1

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Reference Sets

Canada English language reference set (foundation metadata concept)

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