FHIR IG analytics| Package | us.nlm.vsac |
| Resource Type | ValueSet |
| Id | ValueSet-2.16.840.1.113762.1.4.1146.2518.json |
| FHIR Version | R4 |
| Source | https://vsac.nlm.nih.gov/valueset/2.16.840.1.113762.1.4.1146.2518/expansion |
| URL | http://cts.nlm.nih.gov/fhir/ValueSet/2.16.840.1.113762.1.4.1146.2518 |
| Version | 20250218 |
| Status | active |
| Date | 2025-02-18T01:09:31-05:00 |
| Name | Trisomy18DisordersSNOMED |
| Title | Trisomy 18 (Disorders) (SNOMED) |
| Realm | us |
| Authority | hl7 |
| Purpose | (Clinical Focus: This set of values contains diagnoses or problems that represent that the patient has Trisomy 18 regardless of the clinical presentation of the condition),(Data Element Scope: Diagnoses or problems documented in a clinical record.),(Inclusion Criteria: Trisomy 18),(Exclusion Criteria: none) |
No resources found
| CodeSystem | |
| sct | SNOMED codes used in this IG |
No narrative content found in resource
{
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"meta": {
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"lastUpdated": "2025-02-18T01:09:30.000-05:00",
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"extension": [
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"valueContactDetail": {
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{
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"valueString": "Trigger,Trisomy_18"
},
{
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"identifier": [
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"name": "Trisomy18DisordersSNOMED",
"title": "Trisomy 18 (Disorders) (SNOMED)",
"status": "active",
"date": "2025-02-18T01:09:31-05:00",
"publisher": "CSTE Steward",
"jurisdiction": [
{
"coding": [
{
"system": "urn:iso:std:iso:3166",
"code": "US"
}
]
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"compose": {
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"display": "Trisomy 18 detected by multiple marker screening (finding)"
},
{
"code": "205623003",
"display": "Trisomy 18 - meiotic nondisjunction (disorder)"
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{
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"display": "Trisomy 18 - mitotic nondisjunction mosaicism (disorder)"
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{
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{
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"display": "Partial trisomy of chromosome 18 (disorder)"
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"display": "Trisomy 18 (morphologic abnormality)"
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"code": "782676009",
"display": "Distal trisomy 18q (disorder)"
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"timestamp": "2025-05-23T18:48:36-04:00",
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