Version 2.78

Descriptions

Triploidy risk refers to the fetus's risk of being affected by triploid syndrome. The risk can be determined by prenatal genetic testing of fetal DNA. Triploid syndrome is caused by the presence of three copies of every chromosome rather than two, for a total of 69 chromosomes rather than the normal 46. The majority of cases are due to two sperm fertilizing a single egg. Most fetuses with triploidy are lost due to miscarriage, and the few infants born with triploidy have multiple birth defects and only survive a few months. [https://www.rarediseases.org] Source: Regenstrief LOINC, NORD: Triploid syndrome

The genetic counselor's comment regarding risk of a specific disorder or group of disorders is used to convey follow-up recommendations or other information related to the risk result and interpretation. Source: Regenstrief LOINC

Basic Part Properties

Part Display Name
Comment on fetal Triploidy risk
Part Type
Component (Describes the core component or analyte measured)
Created On
2014-09-26
Construct for LOINC Short Name
Fet Triploidy risk comment

LOINC Terminology Service (API) using HL7® FHIR® Get Info

CodeSystem lookup
https://fhir.loinc.org/CodeSystem/$lookup?system=http://loinc.org&code=LP185990-1

Language Variants Get Info

Tag Language Translation
zh-CN Chinese (China) 关于胎儿三倍体风险的遗传咨询师意见
Synonyms: 关于胎儿三倍体（三倍性、三体型、三体性、染色体三倍性、三倍态、三倍体、三倍染色体、三倍体染色体）风险（危险性、风险性、危险）的遗传咨询师（遗传病辅导员、基因咨询师、遗传谘询师、基因谘询师）意见（评论、解释、注释、注解、点评）
es-ES Spanish (Spain) Comentario de consejo genético en riesgo de Triploidía
it-IT Italian (Italy) Commento su rischio Triploidia
tr-TR Turkish (Turkey) Triploidy riski genetik danışman önerisi