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- Fetal_warfarin_syndrome abstract "Fetal warfarin syndrome (Dysmorphism due to warfarin, Warfarin embryopathy ) is a condition associated with administration of Warfarin during pregnancy.Associated conditions include hypoplasia of nasal bridge, laryngomalacia, pectus carinatum, congenital heart defects, ventriculomegaly, agenesis of the corpus callosum, stippled epiphyses, telebrachydactyly, and growth retardation.It is also known as "DiSala syndrome". The symptoms areNasal hypoplasia,Depressed nasal bridge,Deep groove between nostril and nasal tip,Stippling of uncalcified epiphyses during first year,Mild hypoplasia of nails,Shortened fingers,Low birth weight,Significant mental retardation,Seizures,Reduced muscle tone,Widely spaced nipples,Deafness,Feeding difficulty,Failure to thrive".
- Fetal_warfarin_syndrome diseasesdb "33178".
- Fetal_warfarin_syndrome icd10 "Q86.0".
- Fetal_warfarin_syndrome icd9 "760.7".
- Fetal_warfarin_syndrome thumbnail Warfarin.svg?width=300.
- Fetal_warfarin_syndrome wikiPageExternalLink www.rightdiagnosis.com.
- Fetal_warfarin_syndrome wikiPageID "4304948".
- Fetal_warfarin_syndrome wikiPageRevisionID "600844784".
- Fetal_warfarin_syndrome caption Warfarin.
- Fetal_warfarin_syndrome diseasesdb "33178".
- Fetal_warfarin_syndrome hasPhotoCollection Fetal_warfarin_syndrome.
- Fetal_warfarin_syndrome icd "760.7".
- Fetal_warfarin_syndrome icd "Q86.0".
- Fetal_warfarin_syndrome name "Fetal warfarin syndrome".
- Fetal_warfarin_syndrome subject Category:Congenital_malformation_due_to_exogenous_toxicity.
- Fetal_warfarin_syndrome type Abnormality114501726.
- Fetal_warfarin_syndrome type Abstraction100002137.
- Fetal_warfarin_syndrome type Anomaly114505821.
- Fetal_warfarin_syndrome type Attribute100024264.
- Fetal_warfarin_syndrome type BirthDefect114465048.
- Fetal_warfarin_syndrome type Condition113920835.
- Fetal_warfarin_syndrome type CongenitalDisorders.
- Fetal_warfarin_syndrome type Defect114464005.
- Fetal_warfarin_syndrome type Disease114070360.
- Fetal_warfarin_syndrome type IllHealth114052046.
- Fetal_warfarin_syndrome type Illness114061805.
- Fetal_warfarin_syndrome type Imperfection114462666.
- Fetal_warfarin_syndrome type PathologicalState114051917.
- Fetal_warfarin_syndrome type PhysicalCondition114034177.
- Fetal_warfarin_syndrome type State100024720.
- Fetal_warfarin_syndrome type Disease.
- Fetal_warfarin_syndrome type AilmentCondition.
- Fetal_warfarin_syndrome type Situation.
- Fetal_warfarin_syndrome comment "Fetal warfarin syndrome (Dysmorphism due to warfarin, Warfarin embryopathy ) is a condition associated with administration of Warfarin during pregnancy.Associated conditions include hypoplasia of nasal bridge, laryngomalacia, pectus carinatum, congenital heart defects, ventriculomegaly, agenesis of the corpus callosum, stippled epiphyses, telebrachydactyly, and growth retardation.It is also known as "DiSala syndrome".".
- Fetal_warfarin_syndrome label "Fetal warfarin syndrome".
- Fetal_warfarin_syndrome sameAs m.09v0vr9.
- Fetal_warfarin_syndrome sameAs Q5445917.
- Fetal_warfarin_syndrome sameAs Q5445917.
- Fetal_warfarin_syndrome sameAs Fetal_warfarin_syndrome.
- Fetal_warfarin_syndrome wasDerivedFrom Fetal_warfarin_syndrome?oldid=600844784.
- Fetal_warfarin_syndrome depiction Warfarin.svg.
- Fetal_warfarin_syndrome isPrimaryTopicOf Fetal_warfarin_syndrome.
- Fetal_warfarin_syndrome name "Fetal warfarin syndrome".
