ValueSet Comparison between https://profiles.ihe.net/PCC/mAPS/ValueSet/Antepartum.Family.History.and.Genetic.Screening.VS vs https://profiles.ihe.net/PCC/mAPS/ValueSet/Antepartum.Family.History.and.Genetic.Screening.VS

Messages

ErrorValueSet.versionValues for version differ: '1.0.0-comment' vs '1.0.0'
InformationValueSet.dateValues for date differ: '2024-06-04T15:28:59-05:00' vs '2024-10-29T20:32:09+00:00'

Metadata

NameValueComments
.compose.inactive
    .compose.lockedDate
      .copyright
        .date2024-06-04T15:28:59-05:002024-10-29T20:32:09+00:00
        • Values Differ
        .descriptionThis value set includes the type of genetic-related risks identified through screening of the patient’s and biological father’s family history.
          .experimentalfalse
            .immutable
              .jurisdiction
                ..jurisdiction[0]http://unstats.un.org/unsd/methods/m49/m49.htm#001
                  .nameAntepartum_Family_History_and_Genetic_Screening_VS
                    .publisherIHE Patient Care Coordination Committee
                      .purpose
                        .statusactive
                          .titleAntepartum Family History and Genetic Screening
                            .urlhttps://profiles.ihe.net/PCC/mAPS/ValueSet/Antepartum.Family.History.and.Genetic.Screening.VS
                              .version1.0.0-comment1.0.0
                              • Values Differ

                              Definition

                              ItemPropertyValueComments
                              .includehttp://snomed.info/sct
                                ..Concept408856003Autism
                                  ..Concept414022008Blood Disorders
                                    ..Concept80544005Canavan Disease
                                      ..Concept409709004Chromosomal Disorder Includes any inherited genetic or chromosomal disorders
                                        ..Concept13213009Congenital Heart Defect
                                          ..Concept190905008Cystic Fibrosis
                                            ..Concept276720006Dysmorphism (Birth Defect) Patient or baby's father has a child with birth defects
                                              ..Concept41040004Down Syndrome
                                                ..Concept29159009Familial Dysautonomia
                                                  ..Concept90935002Hemophilia
                                                    ..Concept58756001Huntington's Chorea
                                                      ..Concept75934005Maternal Metabolic Disorder
                                                        ..Concept91138005Mental Retardation
                                                          ..Concept73297009Muscular Dystrophy
                                                            ..Concept253098009Neural Tube Defect
                                                              ..Concept102878001Recurrent pregnancy loss/stillbirth
                                                                ..Concept417357006Sickle Cell Disease
                                                                  ..Concept16402000Sickle Cell Trait
                                                                    ..Concept111385000Tay-Sachs
                                                                      ..Concept40108008Thalassemia

                                                                        Expansion

                                                                        Unable to generate expansion - see errors