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205699007: Klinefelter's syndrome, XXYY (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
315463017 Klinefelter's syndrome, XXYY en Synonym Active Entire term case sensitive SNOMED CT core module
591103018 Klinefelter's syndrome, XXYY (disorder) en Fully specified name Active Entire term case sensitive SNOMED CT core module
2839318017 Klinefelter syndrome, XXYY 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's syndrome, XXYY Is a Klinefelter syndrome false Inferred relationship Existential restriction modifier
Klinefelter's syndrome, XXYY Occurrence Congenital false Inferred relationship Existential restriction modifier
Klinefelter's syndrome, XXYY Associated morphology Alteration of chromosome structure false Inferred relationship Existential restriction modifier
Klinefelter's syndrome, XXYY Finding site Sex chromosome X false Inferred relationship Existential restriction modifier 1
Klinefelter's syndrome, XXYY Is a Klinefelter's syndrome false Inferred relationship Existential restriction modifier
Klinefelter's syndrome, XXYY Is a Klinefelter's syndrome - male with more than two X chromosomes false Inferred relationship Existential restriction modifier
Klinefelter's syndrome, XXYY Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier 1
Klinefelter's syndrome, XXYY Finding site Sex chromosome X false Inferred relationship Existential restriction modifier 1
Klinefelter's syndrome, XXYY Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier
Klinefelter's syndrome, XXYY Occurrence Congenital false Inferred relationship Existential restriction modifier 1
Klinefelter's syndrome, XXYY Associated morphology Cellular AND/OR subcellular abnormality false Inferred relationship Existential restriction modifier 1
Klinefelter's syndrome, XXYY Finding site Sex chromosome X false Inferred relationship Existential restriction modifier 1
Klinefelter's syndrome, XXYY Is a Klinefelter syndrome true Inferred relationship Existential restriction modifier
Klinefelter's syndrome, XXYY Occurrence Congenital true Inferred relationship Existential restriction modifier 2
Klinefelter's syndrome, XXYY Associated morphology Alteration of chromosome structure true Inferred relationship Existential restriction modifier 2
Klinefelter's syndrome, XXYY 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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