75568-6
Fetal Monosomy X prior risk [Likelihood] Based on maternal age Narrative
Active
Part Description
LP185800-2 Based on maternal age
The fetal risk for having certain disorders, such as Trisomy 21, varies based on maternal age. For such disorders, an individual infant's risk can be estimated based on known population statistics for how many women in a particular age group have an infant born with the condition compared to the total number of pregnancies for that age group. For example, the fetal Trisomy 21 risk is 1 out of 1,000 for a maternal age of 30 and 1 out of 100 for a maternal age of 40.
Source: Regenstrief LOINC
Fully-Specified Name
- Component
- Monosomy X prior risk
- Property
- Likelihood
- Time
- Pt
- System
- ^Fetus
- Scale
- Nar
- Method
- Based on maternal age
Additional Names
- Long Common Name
- Fetal Monosomy X prior risk [Likelihood] Based on maternal age Narrative
- Short Name
- Fet Ms X prior risk from Mat age
- Display Name
- Monosomy X prior risk Based on maternal age Nar (fetus)
- Consumer Name Alpha Get Info
- Fetal Monosomy X Prior Risk
Basic Attributes
- Class
- MOLPATH
- Type
- Laboratory
- First Released
- Version 2.50
- Last Updated
- Version 2.73
- Order vs. Observation
- Both
Member of these Panels
LOINC | Long Common Name |
---|---|
96978-2 | Noninvasive prenatal fetal aneuploidy and 22q11.2 deletion panel - Plasma cell-free+WBC DNA by Dosage of chromosome-specific cfDNA |
75547-0 | Noninvasive prenatal fetal aneuploidy and microdeletion panel based on Plasma cell-free+WBC DNA by Dosage of chromosome-specific circulating cell free (ccf) DNA |
96977-4 | Noninvasive prenatal fetal aneuploidy panel - Plasma cell-free+WBC DNA by Dosage of chromosome-specific cfDNA |
Language Variants Get Info
Tag | Language | Translation |
---|---|---|
es-ES | Spanish (Spain) | Riesgo previo de monosomía X: |
es-MX | Spanish (Mexico) | Riesgo previo de la monosomía X: |
fr-FR | French (France) | Risque prédominant monosomie X: |
it-IT | Italian (Italy) | Monosomia X, rischio preesistente: Synonyms: Patologia molecolare Punto nel tempo (episodio) Rischio preesistente di monosomia X |
zh-CN | Chinese (China) | 单体型 X 先验风险: Synonyms: 分子病理学; |
LOINC Terminology Service (API) using HL7® FHIR® Get Info
Requests to this service require a free LOINC username and password. Below is a sample of the possible capabilities. See the LOINC Terminology Service documentation for more information.
- CodeSystem lookup
- https:
//fhir.loinc.org/CodeSystem/$lookup?system=http: //loinc.org&code=75568-6
LOINC Copyright
Copyright © 2024 Regenstrief Institute, Inc. All Rights Reserved. To the extent included herein, the LOINC table and LOINC codes are copyright © Regenstrief Institute, Inc. and the Logical Observation Identifiers Names and Codes (LOINC) Committee. See https://