Antepartum Summary
0.0.1-current - ci-build
Antepartum Summary, published by IHE Patient Care Coordination Committee. This is not an authorized publication; it is the continuous build for version 0.0.1-current). This version is based on the current content of https://github.com/IHE/PCC.APS/ and changes regularly. See the Directory of published versions
Official URL: https://profiles.ihe.net/PCC/APS/ValueSet/Antepartum.Family.History.and.Genetic.Screening.VS | Version: 0.0.1-current | |||
Draft as of 2023-10-24 | Computable Name: Antepartum_Family_History_and_Genetic_Screening_VS |
TBD
References
This value set is not used here; it may be used elsewhere (e.g. specifications and/or implementations that use this content)
http://snomed.info/sct
Code | Display |
408856003 | Autism |
414022008 | Blood Disorders |
80544005 | Canavan Disease |
409709004 | Chromosomal Disorder Includes any inherited genetic or chromosomal disorders |
13213009 | Congenital Heart Defect |
190905008 | Cystic Fibrosis |
276720006 | Dysmorphism (Birth Defect) Patient or baby's father has a child with birth defects |
41040004 | Down Syndrome |
29159009 | Familial Dysautonomia |
90935002 | Hemophilia |
58756001 | Huntington's Chorea |
75934005 | Maternal Metabolic Disorder |
91138005 | Mental Retardation |
73297009 | Muscular Dystrophy |
253098009 | Neural Tube Defect |
102878001 | Recurrent pregnancy loss/stillbirth |
417357006 | Sickle Cell Disease |
16402000 | Sickle Cell Trait |
111385000 | Tay-Sachs |
40108008 | Thalassemia |
This value set contains 20 concepts
Expansion based on:
Code | System | Display | Inactive |
408856003 | http://snomed.info/sct | Autism | inactive |
414022008 | http://snomed.info/sct | Blood Disorders | |
80544005 | http://snomed.info/sct | Canavan Disease | |
409709004 | http://snomed.info/sct | Chromosomal Disorder Includes any inherited genetic or chromosomal disorders | |
13213009 | http://snomed.info/sct | Congenital Heart Defect | |
190905008 | http://snomed.info/sct | Cystic Fibrosis | |
276720006 | http://snomed.info/sct | Dysmorphism (Birth Defect) Patient or baby's father has a child with birth defects | |
41040004 | http://snomed.info/sct | Down Syndrome | |
29159009 | http://snomed.info/sct | Familial Dysautonomia | |
90935002 | http://snomed.info/sct | Hemophilia | |
58756001 | http://snomed.info/sct | Huntington's Chorea | |
75934005 | http://snomed.info/sct | Maternal Metabolic Disorder | |
91138005 | http://snomed.info/sct | Mental Retardation | inactive |
73297009 | http://snomed.info/sct | Muscular Dystrophy | |
253098009 | http://snomed.info/sct | Neural Tube Defect | |
102878001 | http://snomed.info/sct | Recurrent pregnancy loss/stillbirth | |
417357006 | http://snomed.info/sct | Sickle Cell Disease | |
16402000 | http://snomed.info/sct | Sickle Cell Trait | |
111385000 | http://snomed.info/sct | Tay-Sachs | |
40108008 | http://snomed.info/sct | Thalassemia |
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 |