Source | hl7.fhir.us.vrsandbox#current:null (v4.0.1) |
resourceType | StructureDefinition |
id | Condition-congenital-anomaly-of-newborn |
canonical | http://hl7.org/fhir/us/vrsandbox/StructureDefinition/Condition-congenital-anomaly-of-newborn |
version | 0.1.0 |
status | draft |
publisher | Example Publisher |
name | ConditionCongenitalAnomalyOfNewborn |
title | Condition - Congenital Anomaly of Newborn |
date | 2023-08-29T15:38:31+00:00 |
description | This Condition profile represents information on whether the infant suffered from one or more of a list of known malformations diagnosed prenatally or after delivery. |
jurisdictions | us |
fhirVersion | 4.0.1 |
kind | resource |
abstract | false |
sdTtype | Condition |
derivation | constraint |
base | http://hl7.org/fhir/us/core/StructureDefinition/us-core-condition-problems-health-concerns |
Usages | (none) |
Name | Flags | Card. | Type | Description & Constraints |
---|---|---|---|---|
Condition | USCoreConditionProblemsHealthConcernsProfile | Information on whether the infant suffered from one or more of a list of known malformations diagnosed prenatally or after delivery. | ||
category | 2.. | |||
category:congenitalAnomolyNewborn | S | 1..1 |
Congenital anomalies of the newborn [US Standard Certificate of Live Birth] Required Pattern: At least the following |
|
coding | 1..* | Coding |
Code defined by a terminology system Fixed Value: (complex) |
|
system | 1..1 | uri |
Identity of the terminology system Fixed Value: http://loinc.org |
|
code | 1..1 | code |
Symbol in syntax defined by the system Fixed Value: 73780-9 |
|
code |
The value set contain the list of values use to specify malformations of the newborn diagnosed prenatally or after delivery. Binding: Newborn Congenital Anomalies (NCHS) ( required ): Newborn Congenital Anomalies (NCHS) |
|||
subject | Reference (Patient - Child Vital Records) | |||
Slices for evidence | S | .. 1 | Slice: Unordered, Open by value:code | |
evidence:karyotypePending | S | 0..1 | Karyotype pending if there is a diagnosis of suspected chromosomal disorder or Down syndrome, Trisomy 21. | |
code | S | 1..1 |
Suspected chromosomal disorder or Down Syndrome: Karyotype pending Required Pattern: At least the following |
|
coding | 1..* | Coding |
Code defined by a terminology system Fixed Value: (complex) |
|
system | 1..1 | uri |
Identity of the terminology system Fixed Value: http://snomed.info/sct |
|
code | 1..1 | code |
Symbol in syntax defined by the system Fixed Value: 312948004 |
|
evidence:karyotypeConfirmedAbmormal | S | 0..1 | Karyotype confirmed if there is a diagnosis of suspected chromosomal disorder or Down syndrome, Trisomy 21. | |
code | S | 1..1 |
Suspected chromosomal disorder or Down Syndrome: Karyotype confirmed Required Pattern: At least the following |
|
coding | 1..* | Coding |
Code defined by a terminology system Fixed Value: (complex) |
|
system | 1..1 | uri |
Identity of the terminology system Fixed Value: http://snomed.info/sct |
|
code | 1..1 | code |
Symbol in syntax defined by the system Fixed Value: 442124003 |
|
Documentation for this format |
Produced 08 Sep 2023