ONKI3 | Medical Subject Headings

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Erythroblastosis, Fetal

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Hierarchy:	Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Fetal Diseases ∟ Erythroblastosis, Fetal 36 coordinate concepts 2 subordinate concepts ∟ Hydrops Fetalis \| ∟ Kernicterus ∟ Chorioamnionitis \| ∟ Fetal Alcohol Syndrome \| ∟ Fetal Growth Retardation \| ∟ Fetal Hypoxia \| ∟ Fetal Macrosomia \| ∟ Fetal Nutrition Disorders \| ∟ Meconium Aspiration Syndrome \| ∟ Nuchal Cord \| ∟ Rh Isoimmunization \| ∟ Amniotic Band Syndrome \| ∟ Anemia, Neonatal \| ∟ Asphyxia Neonatorum \| ∟ Birth Injuries \| ∟ Cystic Fibrosis \| ∟ Epilepsy, Benign Neonatal \| ∟ Hemorrhagic Disease of Newborn \| ∟ Hernia, Umbilical \| ∟ Hydrocephalus \| ∟ Hydrophthalmos \| ∟ Hyperbilirubinemia, Neonatal \| ∟ Hyperostosis, Cortical, Congenital \| ∟ Ichthyosis \| ∟ Infant, Premature, Diseases \| ∟ Mobius Syndrome \| ∟ Neonatal Abstinence Syndrome \| ∟ Nystagmus, Congenital \| ∟ Ophthalmia Neonatorum \| ∟ Persistent Fetal Circulation Syndrome \| ∟ Persistent Hyperinsulinemia Hypoglycemia of Infancy \| ∟ Rothmund-Thomson Syndrome \| ∟ Sclerema Neonatorum \| ∟ Severe Combined Immunodeficiency \| ∟ Syphilis, Congenital \| ∟ Thanatophoric Dysplasia \| ∟ Toxoplasmosis, Congenital \| ∟ Wolman Disease Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Infant, Newborn, Diseases ∟ Erythroblastosis, Fetal 36 coordinate concepts 2 subordinate concepts ∟ Hydrops Fetalis \| ∟ Kernicterus ∟ Chorioamnionitis \| ∟ Fetal Alcohol Syndrome \| ∟ Fetal Growth Retardation \| ∟ Fetal Hypoxia \| ∟ Fetal Macrosomia \| ∟ Fetal Nutrition Disorders \| ∟ Meconium Aspiration Syndrome \| ∟ Nuchal Cord \| ∟ Rh Isoimmunization \| ∟ Amniotic Band Syndrome \| ∟ Anemia, Neonatal \| ∟ Asphyxia Neonatorum \| ∟ Birth Injuries \| ∟ Cystic Fibrosis \| ∟ Epilepsy, Benign Neonatal \| ∟ Hemorrhagic Disease of Newborn \| ∟ Hernia, Umbilical \| ∟ Hydrocephalus \| ∟ Hydrophthalmos \| ∟ Hyperbilirubinemia, Neonatal \| ∟ Hyperostosis, Cortical, Congenital \| ∟ Ichthyosis \| ∟ Infant, Premature, Diseases \| ∟ Mobius Syndrome \| ∟ Neonatal Abstinence Syndrome \| ∟ Nystagmus, Congenital \| ∟ Ophthalmia Neonatorum \| ∟ Persistent Fetal Circulation Syndrome \| ∟ Persistent Hyperinsulinemia Hypoglycemia of Infancy \| ∟ Rothmund-Thomson Syndrome \| ∟ Sclerema Neonatorum \| ∟ Severe Combined Immunodeficiency \| ∟ Syphilis, Congenital \| ∟ Thanatophoric Dysplasia \| ∟ Toxoplasmosis, Congenital \| ∟ Wolman Disease Medical Subject Headings (MeSH) ∟ Female Urogenital Diseases and Pregnancy Complications ∟ Pregnancy Complications ∟ Fetal Diseases ∟ Erythroblastosis, Fetal 36 coordinate concepts 2 subordinate concepts ∟ Hydrops Fetalis \| ∟ Kernicterus ∟ Chorioamnionitis \| ∟ Fetal Alcohol Syndrome \| ∟ Fetal Growth Retardation \| ∟ Fetal Hypoxia \| ∟ Fetal Macrosomia \| ∟ Fetal Nutrition Disorders \| ∟ Meconium Aspiration Syndrome \| ∟ Nuchal Cord \| ∟ Rh Isoimmunization \| ∟ Amniotic Band Syndrome \| ∟ Anemia, Neonatal \| ∟ Asphyxia Neonatorum \| ∟ Birth Injuries \| ∟ Cystic Fibrosis \| ∟ Epilepsy, Benign Neonatal \| ∟ Hemorrhagic Disease of Newborn \| ∟ Hernia, Umbilical \| ∟ Hydrocephalus \| ∟ Hydrophthalmos \| ∟ Hyperbilirubinemia, Neonatal \| ∟ Hyperostosis, Cortical, Congenital \| ∟ Ichthyosis \| ∟ Infant, Premature, Diseases \| ∟ Mobius Syndrome \| ∟ Neonatal Abstinence Syndrome \| ∟ Nystagmus, Congenital \| ∟ Ophthalmia Neonatorum \| ∟ Persistent Fetal Circulation Syndrome \| ∟ Persistent Hyperinsulinemia Hypoglycemia of Infancy \| ∟ Rothmund-Thomson Syndrome \| ∟ Sclerema Neonatorum \| ∟ Severe Combined Immunodeficiency \| ∟ Syphilis, Congenital \| ∟ Thanatophoric Dysplasia \| ∟ Toxoplasmosis, Congenital \| ∟ Wolman Disease Medical Subject Headings (MeSH) ∟ Hemic and Lymphatic Diseases ∟ Hematologic Diseases ∟ Blood Group Incompatibility ∟ Erythroblastosis, Fetal 36 coordinate concepts 2 subordinate concepts ∟ Hydrops Fetalis \| ∟ Kernicterus ∟ Chorioamnionitis \| ∟ Fetal Alcohol Syndrome \| ∟ Fetal Growth Retardation \| ∟ Fetal Hypoxia \| ∟ Fetal Macrosomia \| ∟ Fetal Nutrition Disorders \| ∟ Meconium Aspiration Syndrome \| ∟ Nuchal Cord \| ∟ Rh Isoimmunization \| ∟ Amniotic Band Syndrome \| ∟ Anemia, Neonatal \| ∟ Asphyxia Neonatorum \| ∟ Birth Injuries \| ∟ Cystic Fibrosis \| ∟ Epilepsy, Benign Neonatal \| ∟ Hemorrhagic Disease of Newborn \| ∟ Hernia, Umbilical \| ∟ Hydrocephalus \| ∟ Hydrophthalmos \| ∟ Hyperbilirubinemia, Neonatal \| ∟ Hyperostosis, Cortical, Congenital \| ∟ Ichthyosis \| ∟ Infant, Premature, Diseases \| ∟ Mobius Syndrome \| ∟ Neonatal Abstinence Syndrome \| ∟ Nystagmus, Congenital \| ∟ Ophthalmia Neonatorum \| ∟ Persistent Fetal Circulation Syndrome \| ∟ Persistent Hyperinsulinemia Hypoglycemia of Infancy \| ∟ Rothmund-Thomson Syndrome \| ∟ Sclerema Neonatorum \| ∟ Severe Combined Immunodeficiency \| ∟ Syphilis, Congenital \| ∟ Thanatophoric Dysplasia \| ∟ Toxoplasmosis, Congenital \| ∟ Wolman Disease Medical Subject Headings (MeSH) ∟ Immune System Diseases ∟ Blood Group Incompatibility ∟ Erythroblastosis, Fetal 36 coordinate concepts 2 subordinate concepts ∟ Hydrops Fetalis \| ∟ Kernicterus ∟ Chorioamnionitis \| ∟ Fetal Alcohol Syndrome \| ∟ Fetal Growth Retardation \| ∟ Fetal Hypoxia \| ∟ Fetal Macrosomia \| ∟ Fetal Nutrition Disorders \| ∟ Meconium Aspiration Syndrome \| ∟ Nuchal Cord \| ∟ Rh Isoimmunization \| ∟ Amniotic Band Syndrome \| ∟ Anemia, Neonatal \| ∟ Asphyxia Neonatorum \| ∟ Birth Injuries \| ∟ Cystic Fibrosis \| ∟ Epilepsy, Benign Neonatal \| ∟ Hemorrhagic Disease of Newborn \| ∟ Hernia, Umbilical \| ∟ Hydrocephalus \| ∟ Hydrophthalmos \| ∟ Hyperbilirubinemia, Neonatal \| ∟ Hyperostosis, Cortical, Congenital \| ∟ Ichthyosis \| ∟ Infant, Premature, Diseases \| ∟ Mobius Syndrome \| ∟ Neonatal Abstinence Syndrome \| ∟ Nystagmus, Congenital \| ∟ Ophthalmia Neonatorum \| ∟ Persistent Fetal Circulation Syndrome \| ∟ Persistent Hyperinsulinemia Hypoglycemia of Infancy \| ∟ Rothmund-Thomson Syndrome \| ∟ Sclerema Neonatorum \| ∟ Severe Combined Immunodeficiency \| ∟ Syphilis, Congenital \| ∟ Thanatophoric Dysplasia \| ∟ Toxoplasmosis, Congenital \| ∟ Wolman Disease X
Broader terms:	Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Fetal Diseases ∟ Erythroblastosis, Fetal Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Infant, Newborn, Diseases ∟ Erythroblastosis, Fetal Medical Subject Headings (MeSH) ∟ Female Urogenital Diseases and Pregnancy Complications ∟ Pregnancy Complications ∟ Fetal Diseases ∟ Erythroblastosis, Fetal Medical Subject Headings (MeSH) ∟ Hemic and Lymphatic Diseases ∟ Hematologic Diseases ∟ Blood Group Incompatibility ∟ Erythroblastosis, Fetal Medical Subject Headings (MeSH) ∟ Immune System Diseases ∟ Blood Group Incompatibility ∟ Erythroblastosis, Fetal Fetal Diseases > Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Medical Subject Headings (MeSH) Infant, Newborn, Diseases > Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Medical Subject Headings (MeSH) Fetal Diseases > Pregnancy Complications > Female Urogenital Diseases and Pregnancy Complications > Medical Subject Headings (MeSH) Blood Group Incompatibility > Hematologic Diseases > Hemic and Lymphatic Diseases > Medical Subject Headings (MeSH) Blood Group Incompatibility > Immune System Diseases > Medical Subject Headings (MeSH) X
Narrower terms:	Hydrops Fetalis \| Kernicterus X
Annotation:	erythroblastosis, non-fetal may be ERYTHREMIC MYELOSIS but be careful; do not confuse with HEMORRHAGIC DISEASE OF NEWBORN X
Scope note:	A condition characterized by the abnormal presence of ERYTHROBLASTS in the circulation of the FETUS or NEWBORNS. It is a disorder due to BLOOD GROUP INCOMPATIBILITY, such as the maternal alloimmunization by fetal antigen RH FACTORS leading to HEMOLYSIS of ERYTHROCYTES, hemolytic anemia (ANEMIA, HEMOLYTIC), general edema (HYDROPS FETALIS), and SEVERE JAUNDICE IN NEWBORN. X
activeMeSHYear*:	2006 \| 2007X
dateCreated*:	1999-01-01X
dateRevised*:	2005-06-30X
recordAuthorizer*:	sjnX
recordMaintainer*:	lktX
recordOriginator*:	NLMX
Related term:	Jaundice, Neonatal X
Type:	Concept X
Coordinate terms:	Chorioamnionitis \| Fetal Alcohol Syndrome \| Fetal Growth Retardation \| Fetal Hypoxia \| Fetal Macrosomia \| Fetal Nutrition Disorders \| Meconium Aspiration Syndrome \| Nuchal Cord \| Rh Isoimmunization \| Amniotic Band Syndrome \| Anemia, Neonatal \| Asphyxia Neonatorum \| Birth Injuries \| Cystic Fibrosis \| Epilepsy, Benign Neonatal \| Hemorrhagic Disease of Newborn \| Hernia, Umbilical \| Hydrocephalus \| Hydrophthalmos \| Hyperbilirubinemia, Neonatal \| Hyperostosis, Cortical, Congenital \| Ichthyosis \| Infant, Premature, Diseases \| Mobius Syndrome \| Neonatal Abstinence Syndrome \| Nystagmus, Congenital \| Ophthalmia Neonatorum \| Persistent Fetal Circulation Syndrome \| Persistent Hyperinsulinemia Hypoglycemia of Infancy \| Rothmund-Thomson Syndrome \| Sclerema Neonatorum \| Severe Combined Immunodeficiency \| Syphilis, Congenital \| Thanatophoric Dysplasia \| Toxoplasmosis, Congenital \| Wolman Disease X
URI:	X
Labels and equivalent concepts:	Vastasyntyneen hemolyyttinen tauti (fi) Fetaali erytroblastoosi (fi, replaced) Hemolytisk sjukdom hos nyfödda (sv) Erytroblastosis fetalis (sv, replaced) Fostererytroblastos (sv, replaced) Morbus haemolyticus neonatorum (sv, replaced) Hemolytic Disease of Newborn (en, replaced) Erythroblastosis Fetalis (en, replaced) Morbus haemolyticus neonatorum (la-FI, replaced) Erythroblastosis neonatorum (la-FI, replaced) Erythroblastosis fetalis (la-FI, replaced) X
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