35111009: Trisomy X syndrome (disorder)

SNOMED CT Concept\Clinical finding\Disease\...

\Chromosomal disorder\Congenital disorder due to abnormality of chromosome number OR structure\Anomaly of chromosome pair\Anomaly of sex chromosome\...

\Sex chromosome abnormality - female phenotype\Trisomy X syndrome

\Anomaly of chromosome X\Trisomy X syndrome

\Congenital disease\Congenital disorder due to abnormality of chromosome number OR structure\Anomaly of chromosome pair\Anomaly of sex chromosome\...

\Sex chromosome abnormality - female phenotype\Trisomy X syndrome

\Anomaly of chromosome X\Trisomy X syndrome

Status: current, Sufficiently defined by necessary conditions definition status. Date: 31-Jan 2002. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module

58596018 Trisomy X syndrome en Synonym Active Only initial character case insensitive SNOMED CT core module

58597010 XXX syndrome en Synonym Active Entire term case sensitive SNOMED CT core module

766715016 Trisomy X syndrome (disorder) en Fully specified name Active Only initial character case insensitive SNOMED CT core module

1228248011 Triple X female en Synonym Active Only initial character case insensitive SNOMED CT core module

1228249015 Karyotype 47, XXX en Synonym Active Only initial character case insensitive SNOMED CT core module

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Trisomy X syndrome	Is a	Sex chromosome abnormality - female phenotype	true	Inferred relationship	Existential restriction modifier
Trisomy X syndrome	Is a	Anomaly of chromosome X	true	Inferred relationship	Existential restriction modifier
Trisomy X syndrome	Occurrence	Congenital	false	Inferred relationship	Existential restriction modifier
Trisomy X syndrome	Associated morphology	Alteration of chromosome structure	false	Inferred relationship	Existential restriction modifier
Trisomy X syndrome	Associated morphology	Trisomy	true	Inferred relationship	Existential restriction modifier	1
Trisomy X syndrome	Finding site	Sex chromosome X	true	Inferred relationship	Existential restriction modifier	1
Trisomy X syndrome	Associated morphology	Congenital anomaly	false	Inferred relationship	Existential restriction modifier	1
Trisomy X syndrome	Finding site	Sex chromosome X	false	Inferred relationship	Existential restriction modifier	1
Trisomy X syndrome	Associated morphology	Congenital anomaly	false	Inferred relationship	Existential restriction modifier
Trisomy X syndrome	Occurrence	Congenital	true	Inferred relationship	Existential restriction modifier	1
Trisomy X syndrome	Associated morphology	Cellular AND/OR subcellular abnormality	false	Inferred relationship	Existential restriction modifier	1
Trisomy X syndrome	Finding site	Sex chromosome X	false	Inferred relationship	Existential restriction modifier	1
Trisomy X syndrome	Occurrence	Congenital	false	Inferred relationship	Existential restriction modifier	2
Trisomy X syndrome	Finding site	Sex chromosome X	false	Inferred relationship	Existential restriction modifier	2
Trisomy X syndrome	Associated morphology	Chromosomal morphology	false	Inferred relationship	Existential restriction modifier	2

Inbound Relationships

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Active

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This concept is not in any reference sets