Matches in DBpedia 2016-04 for { <http://dbpedia.org/resource/Lissencephaly> ?p ?o }
- Lissencephaly abstract "Lissencephaly, which literally means smooth brain, is a rare brain formation disorder caused by defective neuronal migration during the 12th to 24th weeks of gestation resulting in a lack of development of brain folds (gyri) and grooves (sulci). It is a form of cephalic disorder. Terms such as 'agyria' (no gyri) or 'pachygyria' (broad gyri) are used to describe the appearance of the surface of the brain. Children with lissencephaly generally have significant developmental delays, but these vary greatly from child to child depending on the degree of brain malformation and seizure control. Life expectancy can be shortened, generally due to respiratory problems.".
- Lissencephaly icd10 "Q04.3".
- Lissencephaly icd9 "742.2".
- Lissencephaly meshId "D054082".
- Lissencephaly omim "607432".
- Lissencephaly thumbnail Lissencephaly.jpg?width=300.
- Lissencephaly wikiPageExternalLink lissencephaly.
- Lissencephaly wikiPageExternalLink liss.
- Lissencephaly wikiPageExternalLink pic.
- Lissencephaly wikiPageExternalLink NBK1185.
- Lissencephaly wikiPageExternalLink NBK5189.
- Lissencephaly wikiPageExternalLink 243310,603937,605755,300067,300121,300067,300121.
- Lissencephaly wikiPageExternalLink uk-lissencephaly.pdf.
- Lissencephaly wikiPageExternalLink lissencephaly_generic_term.html.
- Lissencephaly wikiPageID "232048".
- Lissencephaly wikiPageLength "11810".
- Lissencephaly wikiPageOutDegree "46".
- Lissencephaly wikiPageRevisionID "700111457".
- Lissencephaly wikiPageWikiLink Aristaless_related_homeobox.
- Lissencephaly wikiPageWikiLink Brain.
- Lissencephaly wikiPageWikiLink CT_scan.
- Lissencephaly wikiPageWikiLink Category:Congenital_disorders_of_nervous_system.
- Lissencephaly wikiPageWikiLink Category:Neuronal_migration_disorders.
- Lissencephaly wikiPageWikiLink Cephalic_disorder.
- Lissencephaly wikiPageWikiLink Chorionic_villus_sampling.
- Lissencephaly wikiPageWikiLink Chromosome_17_(human).
- Lissencephaly wikiPageWikiLink Chromosome_7_(human).
- Lissencephaly wikiPageWikiLink Doublecortin.
- Lissencephaly wikiPageWikiLink Epileptic_seizure.
- Lissencephaly wikiPageWikiLink Failure_to_thrive.
- Lissencephaly wikiPageWikiLink Finger.
- Lissencephaly wikiPageWikiLink Fukuyama_congenital_muscular_dystrophy.
- Lissencephaly wikiPageWikiLink Gastrostomy.
- Lissencephaly wikiPageWikiLink Genetic_counseling.
- Lissencephaly wikiPageWikiLink Genetic_testing.
- Lissencephaly wikiPageWikiLink Genetics.
- Lissencephaly wikiPageWikiLink Gestation.
- Lissencephaly wikiPageWikiLink Gyrification.
- Lissencephaly wikiPageWikiLink Gyrus.
- Lissencephaly wikiPageWikiLink Hypotonia.
- Lissencephaly wikiPageWikiLink Magnetic_resonance_imaging.
- Lissencephaly wikiPageWikiLink Microcephaly.
- Lissencephaly wikiPageWikiLink Miller–Dieker_syndrome.
- Lissencephaly wikiPageWikiLink Neuronal_migration_disorder.
- Lissencephaly wikiPageWikiLink Norman–Roberts_syndrome.
- Lissencephaly wikiPageWikiLink Nuclear_magnetic_resonance.
- Lissencephaly wikiPageWikiLink Online_Mendelian_Inheritance_in_Man.
- Lissencephaly wikiPageWikiLink PAFAH1B1.
- Lissencephaly wikiPageWikiLink POMGNT1.
- Lissencephaly wikiPageWikiLink Pachygyria.
- Lissencephaly wikiPageWikiLink Polymicrogyria.
- Lissencephaly wikiPageWikiLink Psychomotor_retardation.
- Lissencephaly wikiPageWikiLink Reelin.
- Lissencephaly wikiPageWikiLink Spasticity.
- Lissencephaly wikiPageWikiLink Sulcus_(neuroanatomy).
- Lissencephaly wikiPageWikiLink TUBA1A.
- Lissencephaly wikiPageWikiLink Toe.
- Lissencephaly wikiPageWikiLink Ultrasound.
- Lissencephaly wikiPageWikiLink Virus.
- Lissencephaly wikiPageWikiLink Walker–Warburg_syndrome.
- Lissencephaly wikiPageWikiLink X_chromosome.
- Lissencephaly wikiPageWikiLink File:Lissencephaly.png.
- Lissencephaly wikiPageWikiLinkText "Lissencephaly".
- Lissencephaly wikiPageWikiLinkText "Lissencephaly#Classification".
- Lissencephaly wikiPageWikiLinkText "agyria".
- Lissencephaly wikiPageWikiLinkText "lissencephalic".
- Lissencephaly wikiPageWikiLinkText "lissencephaly".
- Lissencephaly wikiPageWikiLinkText "smooth-surfaced cerebrum".
- Lissencephaly caption "Lissencephalic brain of human. Lacking surface convolutions .".
- Lissencephaly diseasesdb "29492".
- Lissencephaly genereviewsname "DCX-Related Disorders".
- Lissencephaly genereviewsname "LIS1-Associated Lissencephaly/Subcortical Band Heterotopia".
- Lissencephaly genereviewsnbk "NBK1185".
- Lissencephaly genereviewsnbk "NBK5189".
- Lissencephaly icd "742.2".
- Lissencephaly icd "Q04.3".
- Lissencephaly meshid "D054082".
- Lissencephaly name "Lissencephaly".
- Lissencephaly omim "607432".
- Lissencephaly wikiPageUsesTemplate Template:Commons_category.
- Lissencephaly wikiPageUsesTemplate Template:Congenital_malformations_and_deformations_of_nervous_system.
- Lissencephaly wikiPageUsesTemplate Template:Infobox_disease.
- Lissencephaly wikiPageUsesTemplate Template:NINDS.
- Lissencephaly wikiPageUsesTemplate Template:OMIM2.
- Lissencephaly wikiPageUsesTemplate Template:Redirect-distinguish.
- Lissencephaly wikiPageUsesTemplate Template:Refimprove.
- Lissencephaly wikiPageUsesTemplate Template:Reflist.
- Lissencephaly wikiPageUsesTemplate coregulator_deficiencies.
- Lissencephaly subject Category:Congenital_disorders_of_nervous_system.
- Lissencephaly subject Category:Neuronal_migration_disorders.
- Lissencephaly hypernym Disorder.
- Lissencephaly type Disease.
- Lissencephaly type Disorder.
- Lissencephaly type Redirect.
- Lissencephaly type Thing.
- Lissencephaly type Q12136.
- Lissencephaly comment "Lissencephaly, which literally means smooth brain, is a rare brain formation disorder caused by defective neuronal migration during the 12th to 24th weeks of gestation resulting in a lack of development of brain folds (gyri) and grooves (sulci). It is a form of cephalic disorder. Terms such as 'agyria' (no gyri) or 'pachygyria' (broad gyri) are used to describe the appearance of the surface of the brain.".
- Lissencephaly label "Lissencephaly".
- Lissencephaly differentFrom Argyria.
- Lissencephaly sameAs Q1544416.