Matches in DBpedia 2016-04 for { <http://dbpedia.org/resource/1p36_deletion_syndrome> ?p ?o }
- 1p36_deletion_syndrome abstract "1p36 deletion syndrome (also known as monosomy 1p36) is a congenital genetic disorder characterized by moderate to severe intellectual disability, delayed growth, hypotonia, seizures, limited speech ability, malformations, hearing and vision impairment, and distinct facial features. The symptoms may vary, depending on the exact location of the chromosomal deletion.The condition is caused by a genetic deletion (loss of a segment of DNA) on the outermost band on the short arm (p) of chromosome 1. It is one of the most common deletion syndromes. It is estimated that the syndrome occurs in one in every 5,000 to 10,000 births. Knowledge of the disorder has increased a great deal over the last decade, mainly because more patients have been accurately diagnosed and described in international medical literature.".
- 1p36_deletion_syndrome thumbnail Facial_Features_of_a_Child_with_1p36_Deletion_Syndromel.png?width=300.
- 1p36_deletion_syndrome wikiPageExternalLink what-is-1p36-deletion-syndrome.
- 1p36_deletion_syndrome wikiPageExternalLink br.fcgi?book=gene&part=del1p36.
- 1p36_deletion_syndrome wikiPageExternalLink uk-1p36.pdf.
- 1p36_deletion_syndrome wikiPageExternalLink 1p36+deletion+syndrome.htm.
- 1p36_deletion_syndrome wikiPageID "6398206".
- 1p36_deletion_syndrome wikiPageLength "17252".
- 1p36_deletion_syndrome wikiPageOutDegree "70".
- 1p36_deletion_syndrome wikiPageRevisionID "695598386".
- 1p36_deletion_syndrome wikiPageWikiLink Amblyopia.
- 1p36_deletion_syndrome wikiPageWikiLink American_Sign_Language.
- 1p36_deletion_syndrome wikiPageWikiLink Anatomical_terms_of_location.
- 1p36_deletion_syndrome wikiPageWikiLink Base_pair.
- 1p36_deletion_syndrome wikiPageWikiLink Breast_cancer.
- 1p36_deletion_syndrome wikiPageWikiLink Cataract.
- 1p36_deletion_syndrome wikiPageWikiLink Category:Autosomal_monosomies_and_deletions.
- 1p36_deletion_syndrome wikiPageWikiLink Cerebral_atrophy.
- 1p36_deletion_syndrome wikiPageWikiLink Cervical_cancer.
- 1p36_deletion_syndrome wikiPageWikiLink Chromosome_1_(human).
- 1p36_deletion_syndrome wikiPageWikiLink Cleft_lip_and_palate.
- 1p36_deletion_syndrome wikiPageWikiLink Cochlea.
- 1p36_deletion_syndrome wikiPageWikiLink Colorectal_cancer.
- 1p36_deletion_syndrome wikiPageWikiLink Conductive_hearing_loss.
- 1p36_deletion_syndrome wikiPageWikiLink Congenital_disorder.
- 1p36_deletion_syndrome wikiPageWikiLink Congenital_heart_defect.
- 1p36_deletion_syndrome wikiPageWikiLink Cryptorchidism.
- 1p36_deletion_syndrome wikiPageWikiLink Cyanosis.
- 1p36_deletion_syndrome wikiPageWikiLink Deletion_(genetics).
- 1p36_deletion_syndrome wikiPageWikiLink Developmental_disability.
- 1p36_deletion_syndrome wikiPageWikiLink Dilated_cardiomyopathy.
- 1p36_deletion_syndrome wikiPageWikiLink Dysphagia.
- 1p36_deletion_syndrome wikiPageWikiLink Epilepsy.
- 1p36_deletion_syndrome wikiPageWikiLink Fluorescence_in_situ_hybridization.
- 1p36_deletion_syndrome wikiPageWikiLink Fontanelle.
- 1p36_deletion_syndrome wikiPageWikiLink Gamete.
- 1p36_deletion_syndrome wikiPageWikiLink Genetic_disorder.
- 1p36_deletion_syndrome wikiPageWikiLink Hearing_loss.
- 1p36_deletion_syndrome wikiPageWikiLink Hepatocellular_carcinoma.
- 1p36_deletion_syndrome wikiPageWikiLink Hydrocephalus.
- 1p36_deletion_syndrome wikiPageWikiLink Hyperopia.
- 1p36_deletion_syndrome wikiPageWikiLink Hyperreflexia.
- 1p36_deletion_syndrome wikiPageWikiLink Hypoplasia.
- 1p36_deletion_syndrome wikiPageWikiLink Hypothyroidism.
- 1p36_deletion_syndrome wikiPageWikiLink Hypotonia.
- 1p36_deletion_syndrome wikiPageWikiLink Intellectual_disability.
- 1p36_deletion_syndrome wikiPageWikiLink Kyphoscoliosis.
- 1p36_deletion_syndrome wikiPageWikiLink Kyphosis.
- 1p36_deletion_syndrome wikiPageWikiLink Lacrimal_gland.
- 1p36_deletion_syndrome wikiPageWikiLink Learning_disability.
- 1p36_deletion_syndrome wikiPageWikiLink Lung_cancer.
- 1p36_deletion_syndrome wikiPageWikiLink Melanoma.
- 1p36_deletion_syndrome wikiPageWikiLink Microcephaly.
- 1p36_deletion_syndrome wikiPageWikiLink Music_therapy.
- 1p36_deletion_syndrome wikiPageWikiLink Neoplasm.
- 1p36_deletion_syndrome wikiPageWikiLink Neuroblastoma.
- 1p36_deletion_syndrome wikiPageWikiLink Non-Hodgkin_lymphoma.
- 1p36_deletion_syndrome wikiPageWikiLink Nystagmus.
- 1p36_deletion_syndrome wikiPageWikiLink Ovarian_cancer.
- 1p36_deletion_syndrome wikiPageWikiLink Patent_ductus_arteriosus.
- 1p36_deletion_syndrome wikiPageWikiLink Physical_therapy.
- 1p36_deletion_syndrome wikiPageWikiLink Polyphagia.
- 1p36_deletion_syndrome wikiPageWikiLink Prader–Willi_syndrome.
- 1p36_deletion_syndrome wikiPageWikiLink Prostate_cancer.
- 1p36_deletion_syndrome wikiPageWikiLink Puberty.
- 1p36_deletion_syndrome wikiPageWikiLink Refractive_error.
- 1p36_deletion_syndrome wikiPageWikiLink Sensorineural_hearing_loss.
- 1p36_deletion_syndrome wikiPageWikiLink Shawl_scrotum.
- 1p36_deletion_syndrome wikiPageWikiLink Sixth_nerve_palsy.
- 1p36_deletion_syndrome wikiPageWikiLink Strabismus.
- 1p36_deletion_syndrome wikiPageWikiLink Telomere.
- 1p36_deletion_syndrome wikiPageWikiLink Tetralogy_of_Fallot.
- 1p36_deletion_syndrome wikiPageWikiLink Ventricle_(heart).
- 1p36_deletion_syndrome wikiPageWikiLink Ventricular_septal_defect.
- 1p36_deletion_syndrome wikiPageWikiLink Ventricular_system.
- 1p36_deletion_syndrome wikiPageWikiLink Vestibulocochlear_nerve.
- 1p36_deletion_syndrome wikiPageWikiLink File:Chromosome1.PNG.
- 1p36_deletion_syndrome wikiPageWikiLinkText "1p36 deletion syndrome".
- 1p36_deletion_syndrome wikiPageWikiLinkText "1p36.33".
- 1p36_deletion_syndrome caption "A toddler showing facial symptoms of the syndrome.".
- 1p36_deletion_syndrome diseasesdb "34535".
- 1p36_deletion_syndrome name "1".
- 1p36_deletion_syndrome omim "607872".
- 1p36_deletion_syndrome wikiPageUsesTemplate Template:DECIPHER.
- 1p36_deletion_syndrome wikiPageUsesTemplate Template:Infobox_Disease.
- 1p36_deletion_syndrome wikiPageUsesTemplate Template:Reflist.
- 1p36_deletion_syndrome wikiPageUsesTemplate Template:Research_help.
- 1p36_deletion_syndrome subject Category:Autosomal_monosomies_and_deletions.
- 1p36_deletion_syndrome hypernym Disorder.
- 1p36_deletion_syndrome type Disease.
- 1p36_deletion_syndrome type Redirect.
- 1p36_deletion_syndrome comment "1p36 deletion syndrome (also known as monosomy 1p36) is a congenital genetic disorder characterized by moderate to severe intellectual disability, delayed growth, hypotonia, seizures, limited speech ability, malformations, hearing and vision impairment, and distinct facial features. The symptoms may vary, depending on the exact location of the chromosomal deletion.The condition is caused by a genetic deletion (loss of a segment of DNA) on the outermost band on the short arm (p) of chromosome 1.".
- 1p36_deletion_syndrome label "1p36 deletion syndrome".
- 1p36_deletion_syndrome sameAs Q3297103.
- 1p36_deletion_syndrome sameAs Síndrome_de_supresión_1p36.
- 1p36_deletion_syndrome sameAs Monosomie_1p36.
- 1p36_deletion_syndrome sameAs Zespół_monosomii_1p36.
- 1p36_deletion_syndrome sameAs Sindrome_de_deleção_do_1p36.
- 1p36_deletion_syndrome sameAs m.0g3xpp.
- 1p36_deletion_syndrome sameAs Q3297103.