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205698004: Klinefelter syndrome, male with 46,XX karyotype (disorder)

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

Descriptions:

Id Description Lang Type Status Case? Module
4008377013 Klinefelter syndrome, male with 46,XX karyotype (disorder) en Fully specified name Active Entire term case sensitive SNOMED CT core module
4008378015 Klinefelter's syndrome, male with 46,XX karyotype en Synonym Active Entire term case sensitive SNOMED CT core module
4008379011 Klinefelter syndrome, male with 46,XX karyotype en Synonym Active Entire term case sensitive SNOMED CT core module

0 descendants.

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Klinefelter syndrome, male with 46,XX karyotype Is a XX males true Inferred relationship Existential restriction modifier
Klinefelter syndrome, male with 46,XX karyotype Finding site Male structure false Inferred relationship Existential restriction modifier
Klinefelter syndrome, male with 46,XX karyotype Occurrence Congenital false Inferred relationship Existential restriction modifier
Klinefelter syndrome, male with 46,XX karyotype Finding site Sex chromosome X false Inferred relationship Existential restriction modifier 1
Klinefelter syndrome, male with 46,XX karyotype Associated morphology Alteration of chromosome structure false Inferred relationship Existential restriction modifier
Klinefelter syndrome, male with 46,XX karyotype Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier 1
Klinefelter syndrome, male with 46,XX karyotype Finding site Sex chromosome X false Inferred relationship Existential restriction modifier 1
Klinefelter syndrome, male with 46,XX karyotype Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier
Klinefelter syndrome, male with 46,XX karyotype Occurrence Congenital false Inferred relationship Existential restriction modifier 1
Klinefelter syndrome, male with 46,XX karyotype Associated morphology Cellular AND/OR subcellular abnormality false Inferred relationship Existential restriction modifier 1
Klinefelter syndrome, male with 46,XX karyotype Finding site Sex chromosome X false Inferred relationship Existential restriction modifier 1
Klinefelter syndrome, male with 46,XX karyotype Occurrence Congenital true Inferred relationship Existential restriction modifier 2
Klinefelter syndrome, male with 46,XX karyotype Associated morphology Chromosomal morphology true Inferred relationship Existential restriction modifier 2
Klinefelter syndrome, male with 46,XX karyotype Finding site Sex chromosome X true Inferred relationship Existential restriction modifier 2
Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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