Mobile Antepartum Summary
1.0.0 - trial-use International flag

Mobile Antepartum Summary, published by IHE Patient Care Coordination Committee. This guide is not an authorized publication; it is the continuous build for version 1.0.0 built by the FHIR (HL7® FHIR® Standard) CI Build. This version is based on the current content of https://github.com/IHE/PCC.mAPS/ and changes regularly. See the Directory of published versions

ValueSet: Antepartum Family History and Genetic Screening

Official URL: https://profiles.ihe.net/PCC/mAPS/ValueSet/Antepartum.Family.History.and.Genetic.Screening.VS Version: 1.0.0
Active as of 2025-10-30 Computable Name: Antepartum_Family_History_and_Genetic_Screening_VS

This value set includes the type of genetic-related risks identified through screening of the patient’s and biological father’s family history.

References

Logical Definition (CLD)

 

Expansion

Expansion from tx.fhir.org based on SNOMED CT International edition 01-Feb 2025

This value set contains 20 concepts

SystemCodeDisplay (en)InactivestatusJSONXML
http://snomed.info/sct  408856003Autistic disorder (disorder)inactiveinactive
http://snomed.info/sct  414022008Disorder of cellular component of blood (disorder)
http://snomed.info/sct  80544005Spongy degeneration of central nervous system
http://snomed.info/sct  409709004Chromosomal disorder (disorder)
http://snomed.info/sct  13213009Congenital heart disease
http://snomed.info/sct  190905008Cystic fibrosis
http://snomed.info/sct  276720006Dysmorphism
http://snomed.info/sct  41040004Complete trisomy 21 syndrome
http://snomed.info/sct  29159009Familial dysautonomia
http://snomed.info/sct  90935002Hemophilia
http://snomed.info/sct  58756001Huntington's chorea
http://snomed.info/sct  75934005Metabolic disease
http://snomed.info/sct  91138005Mental retardationinactiveinactive
http://snomed.info/sct  73297009Muscular dystrophy
http://snomed.info/sct  253098009Neural tube defect
http://snomed.info/sct  102878001Recurrent abortion
http://snomed.info/sct  417357006Sickling disorder due to hemoglobin S (disorder)
http://snomed.info/sct  16402000Sickle cell trait
http://snomed.info/sct  111385000Tay-Sachs disease
http://snomed.info/sct  40108008Thalassemia

Explanation of the columns that may appear on this page:

Level A few code lists that FHIR defines are hierarchical - each code is assigned a level. In this scheme, some codes are under other codes, and imply that the code they are under also applies
System The source of the definition of the code (when the value set draws in codes defined elsewhere)
Code The code (used as the code in the resource instance)
Display The display (used in the display element of a Coding). If there is no display, implementers should not simply display the code, but map the concept into their application
Definition An explanation of the meaning of the concept
Comments Additional notes about how to use the code