FHIR IG analytics
| Package | us.nlm.vsac |
| Resource Type | ValueSet |
| Id | ValueSet-2.16.840.1.113762.1.4.1029.129.json |
| FHIR Version | R4 |
| Source | 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 |
| 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
| CodeSystem |
| sct | SNOMED codes used in this IG |
Narrative
No narrative content found in resource
Source1
{
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"name": "FetalConditions",
"title": "Fetal Conditions",
"status": "active",
"date": "2024-06-06T01:23:01-04:00",
"publisher": "Joint Commission",
"jurisdiction": [
{
"coding": [
{
"system": "urn:iso:std:iso:3166",
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"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.)",
"compose": {
"include": [
{
"system": "http://snomed.info/sct",
"concept": [
{
"code": "1142031005",
"display": "Optic atrophy due to late congenital syphilis (disorder)"
},
{
"code": "1142092000",
"display": "Late congenital syphilitic osteochondropathy (disorder)"
},
{
"code": "1142095003",
"display": "Late congenital syphilis of cardiovascular system (disorder)"
},
{
"code": "1193528006",
"display": "Perinatal disorder of fetus and/or neonate due to abnormality of amnion (disorder)"
},
{
"code": "1193537006",
"display": "Early neonatal disorder due to placental insufficiency (disorder)"
},
{
"code": "1197062001",
"display": "Perinatal disorder of fetus and/or early neonate due to placenta previa (disorder)"
},
{
"code": "1197128003",
"display": "Fetal and/or early neonatal disorder due to placental abruption (disorder)"
},
{
"code": "1208944008",
"display": "Early neonatal disorder due to placental abruption (disorder)"
},
{
"code": "1208945009",
"display": "Fetal disorder due to placental abruption (disorder)"
},
{
"code": "1208946005",
"display": "Early neonatal disorder due to placental hemorrhage (disorder)"
},
{
"code": "1208947001",
"display": "Fetal disorder due to placental hemorrhage (disorder)"
},
{
"code": "1222666002",
"display": "Ephrin receptor B4-related lymphatic-related hydrops fetalis (disorder)"
},
{
"code": "1222667006",
"display": "Piezo type mechanosensitive ion channel component 1-related generalized lymphatic dysplasia with non-immune hydrops fetalis (disorder)"
},
{
"code": "1237443008",
"display": "Birth weight 1.5 kilogram or less (finding)"
},
{
"code": "1237576009",
"display": "Baby premature at delivery less than 32 weeks (finding)"
},
{
"code": "1285655009",
"display": "Mild hereditary factor VIII deficiency disease with high response inhibitor (disorder)"
},
{
"code": "1285656005",
"display": "Mild hereditary factor VIII deficiency disease with low response inhibitor (disorder)"
},
{
"code": "1285657001",
"display": "Severe hereditary factor VIII deficiency disease with high response inhibitor (disorder)"
},
{
"code": "1285658006",
"display": "Severe hereditary factor VIII deficiency disease with low response inhibitor (disorder)"
},
{
"code": "1285659003",
"display": "Moderate hereditary factor VIII deficiency disease with high response inhibitor (disorder)"
},
{
"code": "1285660008",
"display": "Moderate hereditary factor VIII deficiency disease with low response inhibitor (disorder)"
},
{
"code": "13993001",
"display": "Factor XIII inhibitor disorder (disorder)"
},
{
"code": "154818001",
"display": "Congenital afibrinogenemia (disorder)"
},
{
"code": "15539009",
"display": "Hydrops fetalis due to isoimmunization (disorder)"
},
{
"code": "15635291000119101",
"display": "Baby premature 35 weeks (finding)"
},
{
"code": "15635331000119107",
"display": "Baby premature 34 weeks (finding)"
},
{
"code": "15635371000119105",
"display": "Baby premature 33 weeks (finding)"
},
{
"code": "15635411000119106",
"display": "Baby premature 32 weeks (finding)"
},
{
"code": "15635451000119107",
"display": "Baby premature 31 weeks (finding)"
},
{
"code": "15750001000119103",
"display": "Baby premature 28 weeks (finding)"
},
{
"code": "15750041000119101",
"display": "Baby premature 29 weeks (finding)"
},
{
"code": "15750081000119106",
"display": "Baby premature 30 weeks (finding)"
},
{
"code": "15887011000119107",
"display": "Baby premature 24 weeks (finding)"
},
{
"code": "15887051000119108",
"display": "Baby premature 25 weeks (finding)"
},
{
"code": "15887091000119103",
"display": "Baby premature 26 weeks (finding)"
},
{
"code": "15887131000119101",
"display": "Baby premature 27 weeks (finding)"
},
{
"code": "16872008",
"display": "Severe hereditary factor VIII deficiency disease (disorder)"
},
{
"code": "16922007",
"display": "Hereditary coagulation factor deficiency (disorder)"
},
{
"code": "169860002",
"display": "Baby birth weight under 3 percent (under 2500g) (finding)"
},
{
"code": "1857005",
"display": "Congenital rubella syndrome (disorder)"
},
{
"code": "18604004",
"display": "Factor XIII deficiency disease (disorder)"
},
{
"code": "186833000",
"display": "Early congenital syphilis - latent (disorder)"
},
{
"code": "186842007",
"display": "Late congenital syphilitic oculopathy (disorder)"
},
{
"code": "199612005",
"display": "Small-for-dates baby (disorder)"
},
{
"code": "206372007",
"display": "Congenital viral hepatitis (disorder)"
},
{
"code": "206373002",
"display": "Congenital hepatitis A infection (disorder)"
},
{
"code": "234442002",
"display": "Hereditary factor VIII deficiency disease with inhibitor (disorder)"
},
{
"code": "234444001",
"display": "Congenital factor IX deficiency variant (disorder)"
},
{
"code": "234445000",
"display": "Congenital factor IX deficiency with inhibitor (disorder)"
},
{
"code": "240487007",
"display": "Congenital parvoviral infection (disorder)"
},
{
"code": "240551003",
"display": "Chronic congenital cytomegalic inclusion disease (disorder)"
},
{
"code": "24149006",
"display": "Hemorrhagic disease of the newborn due to factor II deficiency (disorder)"
},
{
"code": "26029002",
"display": "Mild hereditary factor VIII deficiency disease (disorder)"
},
{
"code": "266125005",
"display": "Early congenital syphilis with symptoms (disorder)"
},
{
"code": "268868001",
"display": "Born very premature (disorder)"
},
{
"code": "275376007",
"display": "Congenital syphilitic chronic coryza (disorder)"
},
{
"code": "27648007",
"display": "Congenital syphilitic periostitis (disorder)"
},
{
"code": "276610007",
"display": "Low birth weight infant (disorder)"
},
{
"code": "276611006",
"display": "Very low birth weight infant (disorder)"
},
{
"code": "276612004",
"display": "Extremely low birth weight infant (disorder)"
},
{
"code": "276658003",
"display": "Extreme immaturity (disorder)"
},
{
"code": "276660001",
"display": "Congenital viral disease (disorder)"
},
{
"code": "276664005",
"display": "Congenital coxsackie infection (disorder)"
},
{
"code": "276665006",
"display": "Congenital acquired immune deficiency syndrome (disorder)"
},
{
"code": "276666007",
"display": "Congenital human immunodeficiency virus positive status syndrome (disorder)"
},
{
"code": "276671000",
"display": "Congenital falciparum malaria (disorder)"
},
{
"code": "276700005",
"display": "Congenital syphilitic rhinitis (disorder)"
},
{
"code": "277644009",
"display": "Congenital varicella syndrome (disorder)"
},
{
"code": "278929008",
"display": "Congenital hepatitis C infection (disorder)"
},
{
"code": "28293008",
"display": "Hereditary factor VIII deficiency disease (disorder)"
},
{
"code": "302811004",
"display": "Progressive congenital rubella encephalomyelitis (disorder)"
},
{
"code": "307333004",
"display": "Rhesus isoimmunization due to anti-D (disorder)"
},
{
"code": "307334005",
"display": "Rhesus isoimmunization due to anti-c (disorder)"
},
{
"code": "307335006",
"display": "Rhesus isoimmunization due to anti-E (disorder)"
},
{
"code": "307336007",
"display": "Rhesus isoimmunization due to anti-Cw (disorder)"
},
{
"code": "310491007",
"display": "Baby birth weight less than 751gm (finding)"
},
{
"code": "310492000",
"display": "Baby birth weight equal to 751g-1kg (finding)"
},
{
"code": "310493005",
"display": "Baby birth weight 1 to 1.5 kilogram (finding)"
},
{
"code": "310494004",
"display": "Baby birth weight 1.5 to 2 kilogram (finding)"
},
{
"code": "310523002",
"display": "Baby premature 24-26 weeks (finding)"
},
{
"code": "310530008",
"display": "Baby premature 36 weeks (finding)"
},
{
"code": "310538001",
"display": "Baby birth weight 2 to 2.5 kilogram (finding)"
},
{
"code": "310548004",
"display": "Baby premature 26-28 weeks (finding)"
},
{
"code": "310659001",
"display": "Birth weight 1000-2499 g (finding)"
},
{
"code": "310660006",
"display": "Birth weight 999 g or less (finding)"
},
{
"code": "310661005",
"display": "Premature infant 28-37 weeks (finding)"
},
{
"code": "31925001",
"display": "Hereditary factor I deficiency disease (disorder)"
},
{
"code": "33169001",
"display": "Factor XI deficiency, type II (disorder)"
},
{
"code": "33297000",
"display": "Hereditary factor II deficiency disease (disorder)"
},
{
"code": "33344008",
"display": "Moderate hereditary factor VIII deficiency disease (disorder)"
},
{
"code": "35742006",
"display": "Congenital syphilis (disorder)"
},
{
"code": "37260006",
"display": "Congenital tuberculosis (disorder)"
},
{
"code": "37350004",
"display": "Hereditary factor X deficiency disease (disorder)"
},
{
"code": "395507008",
"display": "Premature infant (finding)"
},
{
"code": "40855001",
"display": "Hereditary factor VII deficiency disease (disorder)"
},
{
"code": "41788008",
"display": "Hereditary factor IX deficiency disease (disorder)"
},
{
"code": "425949001",
"display": "Mild hereditary factor VIII deficiency disease with inhibitor (disorder)"
},
{
"code": "426199009",
"display": "Congenital factor IX deficiency without inhibitor (disorder)"
},
{
"code": "429151000124100",
"display": "Baby premature 35-36 weeks (finding)"
},
{
"code": "4320005",
"display": "Factor V deficiency (disorder)"
},
{
"code": "43217004",
"display": "Hereditary factor XII deficiency disease (disorder)"
},
{
"code": "4359001",
"display": "Early congenital syphilis (less than 2 years) (disorder)"
},
{
"code": "438360006",
"display": "Hereditary factor VIII deficiency disease without inhibitor (disorder)"
},
{
"code": "438372000",
"display": "Hereditary factor IX deficiency disease with inhibitor (disorder)"
},
{
"code": "438373005",
"display": "Severe hereditary factor VIII deficiency disease with inhibitor (disorder)"
},
{
"code": "438599002",
"display": "Moderate hereditary factor VIII deficiency disease with inhibitor (disorder)"
},
{
"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)"
},
{
"code": "439455002",
"display": "Hereditary factor XIII A subunit deficiency (disorder)"
},
{
"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)"
},
{
"code": "440867000",
"display": "Moderate hereditary factor IX deficiency disease with inhibitor (disorder)"
},
{
"code": "440868005",
"display": "Mild hereditary factor IX deficiency disease with inhibitor (disorder)"
},
{
"code": "440993008",
"display": "Severe hereditary factor VIII deficiency disease without inhibitor (disorder)"
},
{
"code": "441006000",
"display": "Moderate hereditary factor VIII deficiency disease without inhibitor (disorder)"
},
{
"code": "441190003",
"display": "Severe hereditary factor IX deficiency disease without inhibitor (disorder)"
},
{
"code": "441191004",
"display": "Moderate hereditary factor IX deficiency disease without inhibitor (disorder)"
},
{
"code": "441192006",
"display": "Mild hereditary factor IX deficiency disease without inhibitor (disorder)"
},
{
"code": "45366001",
"display": "Hereditary dysfibrinogenemia (disorder)"
},
{
"code": "45963004",
"display": "Factor XI deficiency, type III (disorder)"
},
{
"code": "462169004",
"display": "Fetal supraventricular tachycardia with short ventriculoatrial interval (disorder)"
},
{
"code": "462170003",
"display": "Fetal supraventricular tachycardia with long ventriculoatrial interval (disorder)"
},
{
"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)"
},
{
"code": "50189006",
"display": "Hereditary factor XIII deficiency disease (disorder)"
},
{
"code": "51634001",
"display": "Congenital malaria (disorder)"
},
{
"code": "52079000",
"display": "Congenital human immunodeficiency virus infection (disorder)"
},
{
"code": "54069001",
"display": "Congenital syphilitic mucous patches (disorder)"
},
{
"code": "58392004",
"display": "Congenital syphilitic osteochondritis (disorder)"
},
{
"code": "59527008",
"display": "Congenital cytomegalovirus infection (disorder)"
},
{
"code": "59721007",
"display": "Congenital syphilitic pemphigus (disorder)"
},
{
"code": "60498001",
"display": "Congenital viral hepatitis B infection (disorder)"
},
{
"code": "6456007",
"display": "Supraventricular tachycardia (disorder)"
},
{
"code": "700284005",
"display": "Congenital disseminated toxoplasmosis (disorder)"
},
{
"code": "710068006",
"display": "Baby premature 32-36 weeks (finding)"
},
{
"code": "710168009",
"display": "Birth weight less than 500g (finding)"
},
{
"code": "710235005",
"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)"
},
{
"code": "716660007",
"display": "Congenital infection caused by Epstein-Barr virus (disorder)"
},
{
"code": "721583004",
"display": "Mucocutaneous early congenital syphilis (disorder)"
},
{
"code": "722839000",
"display": "Baby premature at delivery less than 23 weeks (finding)"
},
{
"code": "722840003",
"display": "Baby premature at delivery 23 completed weeks (finding)"
},
{
"code": "73893000",
"display": "Congenital toxoplasmosis (disorder)"
},
{
"code": "762725007",
"display": "Congenital infection caused by Zika virus (disorder)"
},
{
"code": "767712006",
"display": "Factor IX deficiency (disorder)"
},
{
"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",
"display": "Congenital syphilitic choroiditis (disorder)"
}
]
}
]
},
"expansion": {
"identifier": "urn:uuid:81149f98-5e65-4336-9cd7-9bd3cd35d581",
"timestamp": "2025-05-23T16:47:34-04:00",
"total": 160,
"contains": [
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "1142031005",
"display": "Optic atrophy due to late congenital syphilis (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "1142092000",
"display": "Late congenital syphilitic osteochondropathy (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "1142095003",
"display": "Late congenital syphilis of cardiovascular system (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "1193528006",
"display": "Perinatal disorder of fetus and/or neonate due to abnormality of amnion (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "1193537006",
"display": "Early neonatal disorder due to placental insufficiency (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "1197062001",
"display": "Perinatal disorder of fetus and/or early neonate due to placenta previa (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "1197128003",
"display": "Fetal and/or early neonatal disorder due to placental abruption (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "1208944008",
"display": "Early neonatal disorder due to placental abruption (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "1208945009",
"display": "Fetal disorder due to placental abruption (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "1208946005",
"display": "Early neonatal disorder due to placental hemorrhage (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "1208947001",
"display": "Fetal disorder due to placental hemorrhage (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "1222666002",
"display": "Ephrin receptor B4-related lymphatic-related hydrops fetalis (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "1222667006",
"display": "Piezo type mechanosensitive ion channel component 1-related generalized lymphatic dysplasia with non-immune hydrops fetalis (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "1237443008",
"display": "Birth weight 1.5 kilogram or less (finding)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "1237576009",
"display": "Baby premature at delivery less than 32 weeks (finding)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "1285655009",
"display": "Mild hereditary factor VIII deficiency disease with high response inhibitor (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "1285656005",
"display": "Mild hereditary factor VIII deficiency disease with low response inhibitor (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "1285657001",
"display": "Severe hereditary factor VIII deficiency disease with high response inhibitor (disorder)"
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}
FHIR
FHIRsmith