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 '2026-01-15T20:35:26+00:00'
WarningValueSet.compose.include[0].concept[1]Code 414022008 display changed from 'Blood Disorders' to 'Disorder of cellular component of blood (disorder)'
WarningValueSet.compose.include[0].concept[2]Code 80544005 display changed from 'Canavan Disease' to 'Spongy degeneration of central nervous system'
WarningValueSet.compose.include[0].concept[3]Code 409709004 display changed from 'Chromosomal Disorder Includes any inherited genetic or chromosomal disorders' to 'Chromosomal disorder (disorder)'
WarningValueSet.compose.include[0].concept[4]Code 13213009 display changed from 'Congenital Heart Defect' to 'Congenital heart disease'
WarningValueSet.compose.include[0].concept[6]Code 276720006 display changed from 'Dysmorphism (Birth Defect) Patient or baby's father has a child with birth defects' to 'Dysmorphism'
WarningValueSet.compose.include[0].concept[11]Code 75934005 display changed from 'Maternal Metabolic Disorder' to 'Metabolic disease'
WarningValueSet.compose.include[0].concept[15]Code 102878001 display changed from 'Recurrent pregnancy loss/stillbirth' to 'Recurrent abortion'
WarningValueSet.compose.include[0].concept[18]Code 111385000 display changed from 'Tay-Sachs' to 'Tay-Sachs disease'

Metadata

NameValueComments
.compose.inactive
    .compose.lockedDate
      .copyright
        .date2024-06-04T15:28:59-05:002026-01-15T20:35:26+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 DisordersDisorder of cellular component of blood (disorder)
                                    ..Concept80544005Canavan DiseaseSpongy degeneration of central nervous system
                                      ..Concept409709004Chromosomal Disorder Includes any inherited genetic or chromosomal disordersChromosomal disorder (disorder)
                                        ..Concept13213009Congenital Heart DefectCongenital heart disease
                                          ..Concept190905008Cystic Fibrosis
                                            ..Concept276720006Dysmorphism (Birth Defect) Patient or baby's father has a child with birth defectsDysmorphism
                                              ..Concept41040004Down Syndrome
                                                ..Concept29159009Familial Dysautonomia
                                                  ..Concept90935002Hemophilia
                                                    ..Concept58756001Huntington's Chorea
                                                      ..Concept75934005Maternal Metabolic DisorderMetabolic disease
                                                        ..Concept91138005Mental Retardation
                                                          ..Concept73297009Muscular Dystrophy
                                                            ..Concept253098009Neural Tube Defect
                                                              ..Concept102878001Recurrent pregnancy loss/stillbirthRecurrent abortion
                                                                ..Concept417357006Sickle Cell Disease
                                                                  ..Concept16402000Sickle Cell Trait
                                                                    ..Concept111385000Tay-SachsTay-Sachs disease
                                                                      ..Concept40108008Thalassemia

                                                                        Expansion

                                                                        Unable to generate expansion - see errors