FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.21  |  FHIR Version n/a  User: [n/a]

275264009: Klinefelter's syndrome XXXXY (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
411224015 Klinefelter's syndrome XXXXY en Synonym Active Entire term case sensitive SNOMED CT core module
668113010 Klinefelter's syndrome XXXXY (disorder) en Fully specified name Active Entire term case sensitive SNOMED CT core module
2838991013 Klinefelter syndrome XXXXY 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 XXXXY Is a Klinefelter's syndrome - male with more than two X chromosomes false Inferred relationship Existential restriction modifier
Klinefelter's syndrome XXXXY Finding site Sex chromosome X false Inferred relationship Existential restriction modifier 1
Klinefelter's syndrome XXXXY Associated morphology Alteration of chromosome structure false Inferred relationship Existential restriction modifier
Klinefelter's syndrome XXXXY Occurrence Congenital false Inferred relationship Existential restriction modifier
Klinefelter's syndrome XXXXY Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier 1
Klinefelter's syndrome XXXXY Finding site Sex chromosome X false Inferred relationship Existential restriction modifier 1
Klinefelter's syndrome XXXXY Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier
Klinefelter's syndrome XXXXY Occurrence Congenital false Inferred relationship Existential restriction modifier 1
Klinefelter's syndrome XXXXY Associated morphology Cellular AND/OR subcellular abnormality false Inferred relationship Existential restriction modifier 1
Klinefelter's syndrome XXXXY Finding site Sex chromosome X false Inferred relationship Existential restriction modifier 1
Klinefelter's syndrome XXXXY Is a Klinefelter syndrome true Inferred relationship Existential restriction modifier
Klinefelter's syndrome XXXXY Occurrence Congenital true Inferred relationship Existential restriction modifier 2
Klinefelter's syndrome XXXXY Associated morphology Alteration of chromosome structure true Inferred relationship Existential restriction modifier 2
Klinefelter's syndrome XXXXY 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

Back to Start