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205665009: Duplication seen only at prometaphase (disorder)

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

Descriptions:

Id Description Lang Type Status Case? Module
315408011 Duplication seen only at prometaphase en Synonym Active Case insensitive SNOMED CT core
591064012 Duplication seen only at prometaphase (disorder) en Fully specified name Active Case insensitive SNOMED CT core

0 descendants.

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Duplication seen only at prometaphase Is a Congenital chromosomal disease true Inferred relationship Some
Duplication seen only at prometaphase Associated morphology Congenital anomaly false Inferred relationship Some 1
Duplication seen only at prometaphase Finding site Chromosome structure false Inferred relationship Some 1
Duplication seen only at prometaphase Finding site Chromosome structure false Inferred relationship Some 1
Duplication seen only at prometaphase Associated morphology Congenital anomaly false Inferred relationship Some
Duplication seen only at prometaphase Occurrence Congenital false Inferred relationship Some
Duplication seen only at prometaphase Associated morphology Alteration of chromosome structure false Inferred relationship Some
Duplication seen only at prometaphase Occurrence Congenital true Inferred relationship Some 1
Duplication seen only at prometaphase Associated morphology Morphologically abnormal structure true Inferred relationship Some 1
Duplication seen only at prometaphase 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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