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205718006: Chimera 46, XX; 46, XY (disorder)

Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
315484010 Chimera 46, XX; 46, XY en Synonym Active Case sensitive SNOMED CT core
591124011 Chimera 46, XX; 46, XY (disorder) en Fully specified name Active Case sensitive SNOMED CT core

0 descendants.

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Chimera 46, XX; 46, XY Is a Congenital chromosomal disease false Inferred relationship Some
Chimera 46, XX; 46, XY Is a Chimera true Inferred relationship Some
Chimera 46, XX; 46, XY Associated morphology Congenital anomaly false Inferred relationship Some 1
Chimera 46, XX; 46, XY Finding site Chromosome structure false Inferred relationship Some 1
Chimera 46, XX; 46, XY Associated morphology Congenital anomaly false Inferred relationship Some
Chimera 46, XX; 46, XY Finding site Chromosome structure false Inferred relationship Some 1
Chimera 46, XX; 46, XY Finding site Fetal structure false Inferred relationship Some
Chimera 46, XX; 46, XY Associated morphology Alteration of chromosome structure false Inferred relationship Some
Chimera 46, XX; 46, XY Occurrence Fetal period false Inferred relationship Some
Chimera 46, XX; 46, XY Occurrence Congenital false Inferred relationship Some
Chimera 46, XX; 46, XY Occurrence Congenital true Inferred relationship Some 1
Chimera 46, XX; 46, XY Associated morphology Morphologically abnormal structure true Inferred relationship Some 1
Chimera 46, XX; 46, XY Finding site Chromosome structure true Inferred relationship Some 1
Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

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