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38847009: XXXXY syndrome (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
65166019 XXXXY syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
775188012 XXXXY syndrome (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core
65166019 XXXXY syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
775188012 XXXXY syndrome (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
775188012 XXXXY syndrome (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core
3436981001000114 49,XXXXY-Syndrom de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6933051000241111 syndrome XXXXY fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6933051000241111 syndrome XXXXY fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3436981001000114 49,XXXXY-Syndrom de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

0 descendants.

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
XXXXY syndrome Is a Anomaly of chromosome X true Inferred relationship Existential restriction modifier (core metadata concept)
XXXXY syndrome Associated morphology Alteration of chromosome structure false Inferred relationship Existential restriction modifier (core metadata concept)
XXXXY syndrome Finding site Sex chromosome X (cell structure) false Inferred relationship Existential restriction modifier (core metadata concept) 1
XXXXY syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept)
XXXXY syndrome Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept) 1
XXXXY syndrome Finding site Sex chromosome X (cell structure) false Inferred relationship Existential restriction modifier (core metadata concept) 1
XXXXY syndrome Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept)
XXXXY syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 1
XXXXY syndrome Associated morphology Cellular AND/OR subcellular abnormality false Inferred relationship Existential restriction modifier (core metadata concept) 1
XXXXY syndrome Finding site Sex chromosome X (cell structure) false Inferred relationship Existential restriction modifier (core metadata concept) 1
XXXXY syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 2
XXXXY syndrome Associated morphology Chromosomal morphology (morphologic abnormality) true Inferred relationship Existential restriction modifier (core metadata concept) 2
XXXXY syndrome 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

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