FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.4-SNAPSHOT  |  FHIR Version n/a  User: [n/a]

275263003: Klinefelter's syndrome XXXY (disorder)


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
411223014 Klinefelter's syndrome XXXY en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
668112017 Klinefelter's syndrome XXXY (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core
2840381012 Klinefelter syndrome XXXY en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
411223014 Klinefelter's syndrome XXXY en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
668112017 Klinefelter's syndrome XXXY (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
668112017 Klinefelter's syndrome XXXY (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core
2840381012 Klinefelter syndrome XXXY en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Klinefelter's syndrome XXXY Is a Klinefelter's syndrome - male with more than two X chromosomes false Inferred relationship Existential restriction modifier (core metadata concept)
Klinefelter's syndrome XXXY Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept)
Klinefelter's syndrome XXXY Associated morphology Alteration of chromosome structure false Inferred relationship Existential restriction modifier (core metadata concept)
Klinefelter's syndrome XXXY Finding site Sex chromosome X (cell structure) false Inferred relationship Existential restriction modifier (core metadata concept) 1
Klinefelter's syndrome XXXY Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept) 1
Klinefelter's syndrome XXXY Finding site Sex chromosome X (cell structure) false Inferred relationship Existential restriction modifier (core metadata concept) 1
Klinefelter's syndrome XXXY Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept)
Klinefelter's syndrome XXXY Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 1
Klinefelter's syndrome XXXY Associated morphology Cellular AND/OR subcellular abnormality false Inferred relationship Existential restriction modifier (core metadata concept) 1
Klinefelter's syndrome XXXY Finding site Sex chromosome X (cell structure) false Inferred relationship Existential restriction modifier (core metadata concept) 1
Klinefelter's syndrome XXXY Is a A male with two or more X chromosomes. true Inferred relationship Existential restriction modifier (core metadata concept)
Klinefelter's syndrome XXXY Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 2
Klinefelter's syndrome XXXY Associated morphology Alteration of chromosome structure true Inferred relationship Existential restriction modifier (core metadata concept) 2
Klinefelter's syndrome XXXY Finding site Sex chromosome X (cell structure) true Inferred relationship Existential restriction modifier (core metadata concept) 2

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

Back to Start