| Source | us.nlm.vsac#0.11.0:null (v4.0.1) |
| resourceType | ValueSet |
| id | 2.16.840.1.113762.1.4.1029.129 |
| canonical | http://cts.nlm.nih.gov/fhir/ValueSet/2.16.840.1.113762.1.4.1029.129 |
| version | 20230608 |
| status | active |
| publisher | Joint Commission |
| name | FetalConditions |
| title | Fetal Conditions |
| date | 2023-06-08T01:01:14-04:00 |
| Usages |
|
This value set contains 159 concepts
| Code | System | Display |
| 1193528006 | http://snomed.info/sct | Perinatal disorder of fetus and/or neonate due to abnormality of amnion (disorder) |
| 1193537006 | http://snomed.info/sct | Early neonatal disorder due to placental insufficiency (disorder) |
| 1193662003 | http://snomed.info/sct | Perinatal disorder due to placental damage due to cesarean section (disorder) |
| 1197061008 | http://snomed.info/sct | Fetal intrapartum and/or early neonatal disorder due to prolapsed cord (disorder) |
| 1197062001 | http://snomed.info/sct | Perinatal disorder of fetus and/or early neonate due to placenta previa (disorder) |
| 1197128003 | http://snomed.info/sct | Fetal and/or early neonatal disorder due to placental abruption (disorder) |
| 1208944008 | http://snomed.info/sct | Early neonatal disorder due to placental abruption (disorder) |
| 1208945009 | http://snomed.info/sct | Fetal disorder due to placental abruption (disorder) |
| 1208946005 | http://snomed.info/sct | Early neonatal disorder due to placental hemorrhage (disorder) |
| 1208947001 | http://snomed.info/sct | Fetal disorder due to placental hemorrhage (disorder) |
| 1222666002 | http://snomed.info/sct | Ephrin receptor B4-related lymphatic-related hydrops fetalis (disorder) |
| 1222667006 | http://snomed.info/sct | Piezo type mechanosensitive ion channel component 1-related generalized lymphatic dysplasia with non-immune hydrops fetalis (disorder) |
| 13993001 | http://snomed.info/sct | Factor XIII inhibitor disorder (disorder) |
| 154818001 | http://snomed.info/sct | Congenital afibrinogenemia (disorder) |
| 15539009 | http://snomed.info/sct | Hydrops fetalis due to isoimmunization (disorder) |
| 15635291000119101 | http://snomed.info/sct | Baby premature 35 weeks (finding) |
| 15635331000119107 | http://snomed.info/sct | Baby premature 34 weeks (finding) |
| 15635371000119105 | http://snomed.info/sct | Baby premature 33 weeks (finding) |
| 15635411000119106 | http://snomed.info/sct | Baby premature 32 weeks (finding) |
| 15635451000119107 | http://snomed.info/sct | Baby premature 31 weeks (finding) |
| 15750001000119103 | http://snomed.info/sct | Baby premature 28 weeks (finding) |
| 15750041000119101 | http://snomed.info/sct | Baby premature 29 weeks (finding) |
| 15750081000119106 | http://snomed.info/sct | Baby premature 30 weeks (finding) |
| 15887011000119107 | http://snomed.info/sct | Baby premature 24 weeks (finding) |
| 15887051000119108 | http://snomed.info/sct | Baby premature 25 weeks (finding) |
| 15887091000119103 | http://snomed.info/sct | Baby premature 26 weeks (finding) |
| 15887131000119101 | http://snomed.info/sct | Baby premature 27 weeks (finding) |
| 16872008 | http://snomed.info/sct | Severe hereditary factor VIII deficiency disease (disorder) |
| 169860002 | http://snomed.info/sct | Baby birth weight under 3 percent (under 2500g) (finding) |
| 1857005 | http://snomed.info/sct | Congenital rubella syndrome (disorder) |
| 18604004 | http://snomed.info/sct | Factor XIII deficiency disease (disorder) |
| 186833000 | http://snomed.info/sct | Early congenital syphilis - latent (disorder) |
| 186842007 | http://snomed.info/sct | Late congenital syphilitic oculopathy (disorder) |
| 199612005 | http://snomed.info/sct | Small-for-dates baby (disorder) |
| 206082002 | http://snomed.info/sct | Fetal or neonatal effect of placental transfusion syndrome (disorder) |
| 206083007 | http://snomed.info/sct | Fetal or neonatal effect of twin-to-twin transplacental transfusion (disorder) |
| 206084001 | http://snomed.info/sct | Fetal or neonatal effect of fetomaternal transplacental transfusion (disorder) |
| 206085000 | http://snomed.info/sct | Fetal or neonatal effect of maternofetal transplacental transfusion (disorder) |
| 206095007 | http://snomed.info/sct | Fetal or neonatal effect of short cord (disorder) |
| 206096008 | http://snomed.info/sct | Fetal or neonatal effect of thrombosis of umbilical cord (disorder) |
| 206097004 | http://snomed.info/sct | Fetal or neonatal effect of varices of cord (disorder) |
| 206098009 | http://snomed.info/sct | Fetal or neonatal effect of velamentous insertion of cord (disorder) |
| 206099001 | http://snomed.info/sct | Fetal or neonatal effect of vasa previa of cord (disorder) |
| 206100009 | http://snomed.info/sct | Fetal or neonatal effect of long cord (disorder) |
| 206372007 | http://snomed.info/sct | Congenital viral hepatitis (disorder) |
| 206373002 | http://snomed.info/sct | Congenital hepatitis A infection (disorder) |
| 234442002 | http://snomed.info/sct | Hereditary factor VIII deficiency disease with inhibitor (disorder) |
| 234444001 | http://snomed.info/sct | Congenital factor IX deficiency variant (disorder) |
| 234445000 | http://snomed.info/sct | Congenital factor IX deficiency with inhibitor (disorder) |
| 240487007 | http://snomed.info/sct | Congenital parvoviral infection (disorder) |
| 240551003 | http://snomed.info/sct | Chronic congenital cytomegalic inclusion disease (disorder) |
| 24149006 | http://snomed.info/sct | Hemorrhagic disease of the newborn due to factor II deficiency (disorder) |
| 26029002 | http://snomed.info/sct | Mild hereditary factor VIII deficiency disease (disorder) |
| 266125005 | http://snomed.info/sct | Early congenital syphilis with symptoms (disorder) |
| 268868001 | http://snomed.info/sct | Born very premature (disorder) |
| 275376007 | http://snomed.info/sct | Congenital syphilitic chronic coryza (disorder) |
| 27648007 | http://snomed.info/sct | Congenital syphilitic periostitis (disorder) |
| 276610007 | http://snomed.info/sct | Low birth weight infant (disorder) |
| 276611006 | http://snomed.info/sct | Very low birth weight infant (disorder) |
| 276612004 | http://snomed.info/sct | Extremely low birth weight infant (disorder) |
| 276658003 | http://snomed.info/sct | Extreme immaturity (disorder) |
| 276660001 | http://snomed.info/sct | Congenital viral disease (disorder) |
| 276664005 | http://snomed.info/sct | Congenital coxsackie infection (disorder) |
| 276665006 | http://snomed.info/sct | Congenital acquired immune deficiency syndrome (disorder) |
| 276666007 | http://snomed.info/sct | Congenital human immunodeficiency virus positive status syndrome (disorder) |
| 276671000 | http://snomed.info/sct | Congenital falciparum malaria (disorder) |
| 276700005 | http://snomed.info/sct | Congenital syphilitic rhinitis (disorder) |
| 277644009 | http://snomed.info/sct | Congenital varicella syndrome (disorder) |
| 278929008 | http://snomed.info/sct | Congenital hepatitis C infection (disorder) |
| 28293008 | http://snomed.info/sct | Hereditary factor VIII deficiency disease (disorder) |
| 302811004 | http://snomed.info/sct | Progressive congenital rubella encephalomyelitis (disorder) |
| 307333004 | http://snomed.info/sct | Rhesus isoimmunization due to anti-D (disorder) |
| 307334005 | http://snomed.info/sct | Rhesus isoimmunization due to anti-c (disorder) |
| 307335006 | http://snomed.info/sct | Rhesus isoimmunization due to anti-E (disorder) |
| 307336007 | http://snomed.info/sct | Rhesus isoimmunization due to anti-Cw (disorder) |
| 310491007 | http://snomed.info/sct | Baby birth weight less than 751gm (finding) |
| 310492000 | http://snomed.info/sct | Baby birth weight equal to 751g-1kg (finding) |
| 310493005 | http://snomed.info/sct | Baby birth weight 1 to 1.5 kilogram (finding) |
| 310494004 | http://snomed.info/sct | Baby birth weight 1.5 to 2 kilogram (finding) |
| 310523002 | http://snomed.info/sct | Baby premature 24-26 weeks (finding) |
| 310530008 | http://snomed.info/sct | Baby premature 36 weeks (finding) |
| 310538001 | http://snomed.info/sct | Baby birth weight 2 to 2.5 kilogram (finding) |
| 310548004 | http://snomed.info/sct | Baby premature 26-28 weeks (finding) |
| 310659001 | http://snomed.info/sct | Birth weight 1000-2499 g (finding) |
| 310660006 | http://snomed.info/sct | Birth weight 999 g or less (finding) |
| 310661005 | http://snomed.info/sct | Premature infant 28-37 weeks (finding) |
| 31925001 | http://snomed.info/sct | Hereditary factor I deficiency disease (disorder) |
| 33169001 | http://snomed.info/sct | Factor XI deficiency, type II (disorder) |
| 33297000 | http://snomed.info/sct | Hereditary factor II deficiency disease (disorder) |
| 33344008 | http://snomed.info/sct | Moderate hereditary factor VIII deficiency disease (disorder) |
| 35742006 | http://snomed.info/sct | Congenital syphilis (disorder) |
| 37260006 | http://snomed.info/sct | Congenital tuberculosis (disorder) |
| 37350004 | http://snomed.info/sct | Hereditary factor X deficiency disease (disorder) |
| 395507008 | http://snomed.info/sct | Premature infant (finding) |
| 40855001 | http://snomed.info/sct | Hereditary factor VII deficiency disease (disorder) |
| 41788008 | http://snomed.info/sct | Hereditary factor IX deficiency disease (disorder) |
| 425949001 | http://snomed.info/sct | Mild hereditary factor VIII deficiency disease with inhibitor (disorder) |
| 426199009 | http://snomed.info/sct | Congenital factor IX deficiency without inhibitor (disorder) |
| 429151000124100 | http://snomed.info/sct | Baby premature 35-36 weeks (finding) |
| 4320005 | http://snomed.info/sct | Factor V deficiency (disorder) |
| 43217004 | http://snomed.info/sct | Hereditary factor XII deficiency disease (disorder) |
| 4359001 | http://snomed.info/sct | Early congenital syphilis (less than 2 years) (disorder) |
| 438360006 | http://snomed.info/sct | Hereditary factor VIII deficiency disease without inhibitor (disorder) |
| 438372000 | http://snomed.info/sct | Hereditary factor IX deficiency disease with inhibitor (disorder) |
| 438373005 | http://snomed.info/sct | Severe hereditary factor VIII deficiency disease with inhibitor (disorder) |
| 438599002 | http://snomed.info/sct | Moderate hereditary factor VIII deficiency disease with inhibitor (disorder) |
| 438792009 | http://snomed.info/sct | Hereditary factor IX deficiency disease without inhibitor (disorder) |
| 438827002 | http://snomed.info/sct | Hereditary thrombophilic dysfibrinogenemia (disorder) |
| 439455002 | http://snomed.info/sct | Hereditary factor XIII A subunit deficiency (disorder) |
| 439459008 | http://snomed.info/sct | Hereditary factor XIII B subunit deficiency (disorder) |
| 439460003 | http://snomed.info/sct | Hereditary factor XIII A subunit and B subunit deficiency (disorder) |
| 440820004 | http://snomed.info/sct | Mild hereditary factor VIII deficiency disease without inhibitor (disorder) |
| 440866009 | http://snomed.info/sct | Severe hereditary factor IX deficiency disease with inhibitor (disorder) |
| 440867000 | http://snomed.info/sct | Moderate hereditary factor IX deficiency disease with inhibitor (disorder) |
| 440868005 | http://snomed.info/sct | Mild hereditary factor IX deficiency disease with inhibitor (disorder) |
| 440993008 | http://snomed.info/sct | Severe hereditary factor VIII deficiency disease without inhibitor (disorder) |
| 441006000 | http://snomed.info/sct | Moderate hereditary factor VIII deficiency disease without inhibitor (disorder) |
| 441190003 | http://snomed.info/sct | Severe hereditary factor IX deficiency disease without inhibitor (disorder) |
| 441191004 | http://snomed.info/sct | Moderate hereditary factor IX deficiency disease without inhibitor (disorder) |
| 441192006 | http://snomed.info/sct | Mild hereditary factor IX deficiency disease without inhibitor (disorder) |
| 45366001 | http://snomed.info/sct | Hereditary dysfibrinogenemia (disorder) |
| 45963004 | http://snomed.info/sct | Factor XI deficiency, type III (disorder) |
| 46235002 | http://snomed.info/sct | Early latent congenital syphilis, positive serology, negative spinal fluid (disorder) |
| 47082005 | http://snomed.info/sct | Congenital rubella pneumonitis (disorder) |
| 49762007 | http://snomed.info/sct | Hereditary factor XI deficiency disease (disorder) |
| 50189006 | http://snomed.info/sct | Hereditary factor XIII deficiency disease (disorder) |
| 51634001 | http://snomed.info/sct | Congenital malaria (disorder) |
| 52079000 | http://snomed.info/sct | Congenital human immunodeficiency virus infection (disorder) |
| 54069001 | http://snomed.info/sct | Congenital syphilitic mucous patches (disorder) |
| 58357007 | http://snomed.info/sct | Fetal or neonatal effect of vasa previa (disorder) |
| 58392004 | http://snomed.info/sct | Congenital syphilitic osteochondritis (disorder) |
| 59527008 | http://snomed.info/sct | Congenital cytomegalovirus infection (disorder) |
| 59721007 | http://snomed.info/sct | Congenital syphilitic pemphigus (disorder) |
| 60498001 | http://snomed.info/sct | Congenital viral hepatitis B infection (disorder) |
| 6456007 | http://snomed.info/sct | Supraventricular tachycardia (disorder) |
| 700284005 | http://snomed.info/sct | Congenital disseminated toxoplasmosis (disorder) |
| 710068006 | http://snomed.info/sct | Baby premature 32-36 weeks (finding) |
| 710168009 | http://snomed.info/sct | Birth weight less than 500g (finding) |
| 710235005 | http://snomed.info/sct | Baby premature 28-32 weeks (finding) |
| 713204000 | http://snomed.info/sct | Non immune hydrops in newborn (disorder) |
| 715337002 | http://snomed.info/sct | Congenital infection caused by Herpes virus (disorder) |
| 716660007 | http://snomed.info/sct | Congenital infection caused by Epstein-Barr virus (disorder) |
| 721583004 | http://snomed.info/sct | Mucocutaneous early congenital syphilis (disorder) |
| 722839000 | http://snomed.info/sct | Baby premature at delivery less than 23 weeks (finding) |
| 722840003 | http://snomed.info/sct | Baby premature at delivery 23 completed weeks (finding) |
| 73893000 | http://snomed.info/sct | Congenital toxoplasmosis (disorder) |
| 762725007 | http://snomed.info/sct | Congenital infection caused by Zika virus (disorder) |
| 767712006 | http://snomed.info/sct | Factor IX deficiency (disorder) |
| 767713001 | http://snomed.info/sct | Factor XI deficiency (disorder) |
| 79303006 | http://snomed.info/sct | Expanded rubella syndrome (disorder) |
| 7964000 | http://snomed.info/sct | Congenital listeriosis (disorder) |
| 81402009 | http://snomed.info/sct | Fetal or neonatal effect of condition of umbilical cord (disorder) |
| 84880007 | http://snomed.info/sct | Fetal or neonatal effect of complication of placenta, cord and/or membranes (disorder) |
| 86986002 | http://snomed.info/sct | Hemolytic disease of fetus OR newborn due to RhD isoimmunization (disorder) |
| 88540000 | http://snomed.info/sct | Factor XI deficiency, type I (disorder) |
| 88776002 | http://snomed.info/sct | Hereditary factor V deficiency disease (disorder) |
| 890097003 | http://snomed.info/sct | Baby premature at delivery less than 26 weeks (finding) |
| 91576008 | http://snomed.info/sct | Congenital herpes simplex (disorder) |
| 9941009 | http://snomed.info/sct | Congenital syphilitic choroiditis (disorder) |
Produced 08 Sep 2023