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- 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 diseasesdb "34535".
- 1p36_deletion_syndrome omim "607872".
- 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 wikiPageRevisionID "606479500".
- 1p36_deletion_syndrome caption "A toddler showing facial symptoms of the syndrome.".
- 1p36_deletion_syndrome diseasesdb "34535".
- 1p36_deletion_syndrome hasPhotoCollection 1p36_deletion_syndrome.
- 1p36_deletion_syndrome name "1".
- 1p36_deletion_syndrome omim "607872".
- 1p36_deletion_syndrome wordnet_type synset-disease-noun-1.
- 1p36_deletion_syndrome subject Category:Autosomal_monosomies_and_deletions.
- 1p36_deletion_syndrome type Disease.
- 1p36_deletion_syndrome type AilmentCondition.
- 1p36_deletion_syndrome type Situation.
- 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 label "Sindrome de deleção do 1p36".
- 1p36_deletion_syndrome label "Síndrome de supresión 1p36".
- 1p36_deletion_syndrome label "Zespół monosomii 1p36".
- 1p36_deletion_syndrome sameAs Síndrome_de_supresión_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.
- 1p36_deletion_syndrome sameAs Q3297103.
- 1p36_deletion_syndrome wasDerivedFrom 1p36_deletion_syndrome?oldid=606479500.
- 1p36_deletion_syndrome depiction Facial_Features_of_a_Child_with_1p36_Deletion_Syndromel.png.
- 1p36_deletion_syndrome isPrimaryTopicOf 1p36_deletion_syndrome.
- 1p36_deletion_syndrome name "1p36 deletion syndrome".