ONKI3 | Medical Subject Headings

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The way property values are displayed: value/row values side by side

The way concept relations are shown: separately in hierarchy

Persistent Fetal Circulation Syndrome

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Hierarchy:	Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Infant, Newborn, Diseases ∟ Persistent Fetal Circulation Syndrome 28 coordinate concepts ∟ Amniotic Band Syndrome \| ∟ Anemia, Neonatal \| ∟ Asphyxia Neonatorum \| ∟ Birth Injuries \| ∟ Cystic Fibrosis \| ∟ Epilepsy, Benign Neonatal \| ∟ Erythroblastosis, Fetal \| ∟ Hemorrhagic Disease of Newborn \| ∟ Hernia, Umbilical \| ∟ Hydrocephalus \| ∟ Hydrophthalmos \| ∟ Hyperbilirubinemia, Neonatal \| ∟ Hyperostosis, Cortical, Congenital \| ∟ Ichthyosis \| ∟ Infant, Premature, Diseases \| ∟ Meconium Aspiration Syndrome \| ∟ Mobius Syndrome \| ∟ Neonatal Abstinence Syndrome \| ∟ Nystagmus, Congenital \| ∟ Ophthalmia Neonatorum \| ∟ 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) ∟ Respiratory Tract Diseases ∟ Lung Diseases ∟ Hypertension, Pulmonary ∟ Persistent Fetal Circulation Syndrome 28 coordinate concepts ∟ Amniotic Band Syndrome \| ∟ Anemia, Neonatal \| ∟ Asphyxia Neonatorum \| ∟ Birth Injuries \| ∟ Cystic Fibrosis \| ∟ Epilepsy, Benign Neonatal \| ∟ Erythroblastosis, Fetal \| ∟ Hemorrhagic Disease of Newborn \| ∟ Hernia, Umbilical \| ∟ Hydrocephalus \| ∟ Hydrophthalmos \| ∟ Hyperbilirubinemia, Neonatal \| ∟ Hyperostosis, Cortical, Congenital \| ∟ Ichthyosis \| ∟ Infant, Premature, Diseases \| ∟ Meconium Aspiration Syndrome \| ∟ Mobius Syndrome \| ∟ Neonatal Abstinence Syndrome \| ∟ Nystagmus, Congenital \| ∟ Ophthalmia Neonatorum \| ∟ 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 ∟ Infant, Newborn, Diseases ∟ Persistent Fetal Circulation Syndrome Medical Subject Headings (MeSH) ∟ Respiratory Tract Diseases ∟ Lung Diseases ∟ Hypertension, Pulmonary ∟ Persistent Fetal Circulation Syndrome Infant, Newborn, Diseases > Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Medical Subject Headings (MeSH) Hypertension, Pulmonary > Lung Diseases > Respiratory Tract Diseases > Medical Subject Headings (MeSH) X
Annotation:	also known as PPHN; check the tags HUMANS & INFANT, NEWBORN; DF: PFC SYNDROME X
History note:	Ductus Arteriosus, Patent (1966-1979) \| Hypertension, Pulmonary (1966-1979) \| Pulmonary Circulation (1966-1979)X
historyNote*:	80 X
publicMeSHNote*:	80 X
Scope note:	A syndrome of persistent PULMONARY HYPERTENSION in the newborn infant (INFANT, NEWBORN) without demonstrable HEART DISEASES. This neonatal condition can be caused by severe pulmonary vasoconstriction (reactive type), hypertrophy of pulmonary arterial muscle (hypertrophic type), or abnormally developed pulmonary arterioles (hypoplastic type). The newborn patient exhibits CYANOSIS and ACIDOSIS due to the persistence of fetal circulatory pattern of right-to-left shunting of blood through a patent ductus arteriosus (DUCTUS ARTERIOSUS, PATENT) and at times a patent foramen ovale (FORAMEN OVALE, PATENT). X
activeMeSHYear*:	2005 \| 2006 \| 2007X
dateCreated*:	1979-02-28X
dateEstablished*:	1980-01-01X
dateRevised*:	2004-07-13X
recordAuthorizer*:	sjnX
recordMaintainer*:	sjnX
recordOriginator*:	AEPX
Type:	Concept X
Coordinate terms:	Amniotic Band Syndrome \| Anemia, Neonatal \| Asphyxia Neonatorum \| Birth Injuries \| Cystic Fibrosis \| Epilepsy, Benign Neonatal \| Erythroblastosis, Fetal \| Hemorrhagic Disease of Newborn \| Hernia, Umbilical \| Hydrocephalus \| Hydrophthalmos \| Hyperbilirubinemia, Neonatal \| Hyperostosis, Cortical, Congenital \| Ichthyosis \| Infant, Premature, Diseases \| Meconium Aspiration Syndrome \| Mobius Syndrome \| Neonatal Abstinence Syndrome \| Nystagmus, Congenital \| Ophthalmia Neonatorum \| 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:	Fetaaliverenkierto-oireyhtymä (fi) Pysyvä sikiön verenkierto -oireyhtymä (fi, replaced) Pysyvä fetaaliverenkierto -syndrooma (fi, replaced) Pysyvä sikiön verenkierto -syndrooma (fi, replaced) Sikiöverenkierron säilyminen (fi, replaced) Syntymän jälkeen jatkuva sikiöverenkierto (fi, replaced) Pysyvä fetaaliverenkierto -oireyhtymä (fi, replaced) PFC (fi, replaced) Persistoiva fetaaliverenkierto (fi, replaced) Fetaaliverenkiertosyndrooma (fi, replaced) Hypertension, Pulmonary, of Newborn, Persistent (en, replaced) Fetal Circulation, Persistent (en, replaced) Persistent Fetal Circulation (en, replaced) Persistent Pulmonary Hypertension of Newborn (en, replaced) Circulation, Persistent Fetal (en, replaced) Circulatio fetalis persistens (la-FI, replaced) X
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