Resource ValueSet/FHIR Server from package us.nlm.vsac#0.21.0 (188 ms)
| Package | us.nlm.vsac |
| Type | ValueSet |
| Id | Id |
| FHIR Version | R4 |
| Source | http://fhir.org/packages/us.nlm.vsac/https://vsac.nlm.nih.gov/valueset/2.16.840.1.113762.1.4.1029.129/expansion |
| Url | http://cts.nlm.nih.gov/fhir/ValueSet/2.16.840.1.113762.1.4.1029.129 |
| Version | 20240606 |
| Status | active |
| Date | 2024-06-06T01:23:01-04:00 |
| Name | FetalConditions |
| Title | Fetal Conditions |
| Experimental | False |
| Realm | us |
| Authority | hl7 |
| Purpose | (Clinical Focus: The purpose of this value set is to identify diagnoses of selected fetal conditions.),(Data Element Scope: This value set may use a model element related to diagnosis.),(Inclusion Criteria: Includes concepts that identify a diagnosis of selected fetal conditions, including low birth weight less than 2500 grams.),(Exclusion Criteria: No exclusions.) |
Resources that use this resource
Resources that this resource uses
Source
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"date" : "2024-06-06T01:23:01-04:00",
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"display" : "Severe hereditary factor VIII deficiency disease with high response inhibitor (disorder)"
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{
"code" : "13993001",
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{
"code" : "154818001",
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{
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{
"code" : "15887131000119101",
"display" : "Baby premature 27 weeks (finding)"
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{
"code" : "16872008",
"display" : "Severe hereditary factor VIII deficiency disease (disorder)"
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{
"code" : "16922007",
"display" : "Hereditary coagulation factor deficiency (disorder)"
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{
"code" : "169860002",
"display" : "Baby birth weight under 3 percent (under 2500g) (finding)"
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{
"code" : "1857005",
"display" : "Congenital rubella syndrome (disorder)"
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{
"code" : "18604004",
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{
"code" : "186833000",
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{
"code" : "186842007",
"display" : "Late congenital syphilitic oculopathy (disorder)"
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{
"code" : "199612005",
"display" : "Small-for-dates baby (disorder)"
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{
"code" : "206372007",
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{
"code" : "206373002",
"display" : "Congenital hepatitis A infection (disorder)"
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{
"code" : "234442002",
"display" : "Hereditary factor VIII deficiency disease with inhibitor (disorder)"
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{
"code" : "234444001",
"display" : "Congenital factor IX deficiency variant (disorder)"
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"display" : "Congenital factor IX deficiency with inhibitor (disorder)"
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{
"code" : "240487007",
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{
"code" : "240551003",
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"code" : "26029002",
"display" : "Mild hereditary factor VIII deficiency disease (disorder)"
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"display" : "Congenital syphilitic periostitis (disorder)"
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"display" : "Low birth weight infant (disorder)"
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{
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"display" : "Congenital syphilitic rhinitis (disorder)"
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{
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{
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"display" : "Hereditary factor VIII deficiency disease (disorder)"
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"display" : "Baby premature 36 weeks (finding)"
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"display" : "Baby birth weight 2 to 2.5 kilogram (finding)"
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{
"code" : "310548004",
"display" : "Baby premature 26-28 weeks (finding)"
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"code" : "310659001",
"display" : "Birth weight 1000-2499 g (finding)"
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"display" : "Birth weight 999 g or less (finding)"
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{
"code" : "310661005",
"display" : "Premature infant 28-37 weeks (finding)"
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{
"code" : "31925001",
"display" : "Hereditary factor I deficiency disease (disorder)"
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{
"code" : "33169001",
"display" : "Factor XI deficiency, type II (disorder)"
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"display" : "Hereditary factor II deficiency disease (disorder)"
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{
"code" : "33344008",
"display" : "Moderate hereditary factor VIII deficiency disease (disorder)"
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{
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"display" : "Congenital syphilis (disorder)"
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{
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"display" : "Congenital tuberculosis (disorder)"
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{
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"display" : "Hereditary factor X deficiency disease (disorder)"
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"display" : "Hereditary factor IX deficiency disease (disorder)"
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"display" : "Mild hereditary factor VIII deficiency disease with inhibitor (disorder)"
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{
"code" : "426199009",
"display" : "Congenital factor IX deficiency without inhibitor (disorder)"
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{
"code" : "429151000124100",
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{
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"display" : "Factor V deficiency (disorder)"
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{
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"display" : "Hereditary factor XII deficiency disease (disorder)"
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{
"code" : "4359001",
"display" : "Early congenital syphilis (less than 2 years) (disorder)"
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{
"code" : "438360006",
"display" : "Hereditary factor VIII deficiency disease without inhibitor (disorder)"
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{
"code" : "438372000",
"display" : "Hereditary factor IX deficiency disease with inhibitor (disorder)"
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{
"code" : "438373005",
"display" : "Severe hereditary factor VIII deficiency disease with inhibitor (disorder)"
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{
"code" : "438599002",
"display" : "Moderate hereditary factor VIII deficiency disease with inhibitor (disorder)"
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{
"code" : "438792009",
"display" : "Hereditary factor IX deficiency disease without inhibitor (disorder)"
},
{
"code" : "438827002",
"display" : "Hereditary thrombophilic dysfibrinogenemia (disorder)"
},
{
"code" : "439157002",
"display" : "Hereditary combined coagulation factor deficiency (disorder)"
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{
"code" : "439455002",
"display" : "Hereditary factor XIII A subunit deficiency (disorder)"
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{
"code" : "439459008",
"display" : "Hereditary factor XIII B subunit deficiency (disorder)"
},
{
"code" : "439460003",
"display" : "Hereditary factor XIII A subunit and B subunit deficiency (disorder)"
},
{
"code" : "440820004",
"display" : "Mild hereditary factor VIII deficiency disease without inhibitor (disorder)"
},
{
"code" : "440866009",
"display" : "Severe hereditary factor IX deficiency disease with inhibitor (disorder)"
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{
"code" : "440867000",
"display" : "Moderate hereditary factor IX deficiency disease with inhibitor (disorder)"
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{
"code" : "440868005",
"display" : "Mild hereditary factor IX deficiency disease with inhibitor (disorder)"
},
{
"code" : "440993008",
"display" : "Severe hereditary factor VIII deficiency disease without inhibitor (disorder)"
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{
"code" : "441006000",
"display" : "Moderate hereditary factor VIII deficiency disease without inhibitor (disorder)"
},
{
"code" : "441190003",
"display" : "Severe hereditary factor IX deficiency disease without inhibitor (disorder)"
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{
"code" : "441191004",
"display" : "Moderate hereditary factor IX deficiency disease without inhibitor (disorder)"
},
{
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"display" : "Mild hereditary factor IX deficiency disease without inhibitor (disorder)"
},
{
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"display" : "Hereditary dysfibrinogenemia (disorder)"
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{
"code" : "45963004",
"display" : "Factor XI deficiency, type III (disorder)"
},
{
"code" : "462169004",
"display" : "Fetal supraventricular tachycardia with short ventriculoatrial interval (disorder)"
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{
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"display" : "Fetal supraventricular tachycardia with long ventriculoatrial interval (disorder)"
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{
"code" : "46235002",
"display" : "Early latent congenital syphilis, positive serology, negative spinal fluid (disorder)"
},
{
"code" : "47082005",
"display" : "Congenital rubella pneumonitis (disorder)"
},
{
"code" : "49762007",
"display" : "Hereditary factor XI deficiency disease (disorder)"
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{
"code" : "50189006",
"display" : "Hereditary factor XIII deficiency disease (disorder)"
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{
"code" : "51634001",
"display" : "Congenital malaria (disorder)"
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{
"code" : "52079000",
"display" : "Congenital human immunodeficiency virus infection (disorder)"
},
{
"code" : "54069001",
"display" : "Congenital syphilitic mucous patches (disorder)"
},
{
"code" : "58392004",
"display" : "Congenital syphilitic osteochondritis (disorder)"
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{
"code" : "59527008",
"display" : "Congenital cytomegalovirus infection (disorder)"
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{
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"display" : "Congenital syphilitic pemphigus (disorder)"
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{
"code" : "60498001",
"display" : "Congenital viral hepatitis B infection (disorder)"
},
{
"code" : "6456007",
"display" : "Supraventricular tachycardia (disorder)"
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{
"code" : "700284005",
"display" : "Congenital disseminated toxoplasmosis (disorder)"
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{
"code" : "710068006",
"display" : "Baby premature 32-36 weeks (finding)"
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{
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"display" : "Birth weight less than 500g (finding)"
},
{
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"display" : "Baby premature 28-32 weeks (finding)"
},
{
"code" : "713204000",
"display" : "Non immune hydrops in newborn (disorder)"
},
{
"code" : "715337002",
"display" : "Congenital infection caused by Herpes virus (disorder)"
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{
"code" : "716660007",
"display" : "Congenital infection caused by Epstein-Barr virus (disorder)"
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{
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{
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"display" : "Baby premature at delivery less than 23 weeks (finding)"
},
{
"code" : "722840003",
"display" : "Baby premature at delivery 23 completed weeks (finding)"
},
{
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"display" : "Congenital toxoplasmosis (disorder)"
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{
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"display" : "Congenital infection caused by Zika virus (disorder)"
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{
"code" : "767712006",
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{
"code" : "767713001",
"display" : "Factor XI deficiency (disorder)"
},
{
"code" : "79303006",
"display" : "Expanded rubella syndrome (disorder)"
},
{
"code" : "7964000",
"display" : "Congenital listeriosis (disorder)"
},
{
"code" : "81060008",
"display" : "Intestinal obstruction (disorder)"
},
{
"code" : "86986002",
"display" : "Hemolytic disease of fetus OR newborn due to RhD isoimmunization (disorder)"
},
{
"code" : "88540000",
"display" : "Factor XI deficiency, type I (disorder)"
},
{
"code" : "88776002",
"display" : "Hereditary factor V deficiency disease (disorder)"
},
{
"code" : "890097003",
"display" : "Baby premature at delivery less than 26 weeks (finding)"
},
{
"code" : "91576008",
"display" : "Congenital herpes simplex (disorder)"
},
{
"code" : "9941009",
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]
},
"expansion" : {
"identifier" : "urn:uuid:f4dec929-fd2c-42dd-9f0f-000e34e40683",
"timestamp" : "2024-12-10T04:36:41-05:00",
"total" : 160,
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"version" : "http://snomed.info/sct/731000124108/version/20240901",
"code" : "1142031005",
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"code" : "1208945009",
"display" : "Fetal disorder due to placental abruption (disorder)"
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"system" : "http://snomed.info/sct",
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"system" : "http://snomed.info/sct",
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"system" : "http://snomed.info/sct",
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"code" : "1222667006",
"display" : "Piezo type mechanosensitive ion channel component 1-related generalized lymphatic dysplasia with non-immune hydrops fetalis (disorder)"
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XIG built as of ??metadata-date??. Found ??metadata-resources?? resources in ??metadata-packages?? packages.
FHIR