Matches in DBpedia 2016-04 for { <http://dbpedia.org/resource/Liebenberg_syndrome> ?p ?o }
Showing triples 1 to 52 of
52
with 100 triples per page.
- Liebenberg_syndrome abstract "Liebenberg Syndrome is a rare autosomal genetic disease that involves a deletion mutation upstream of the PITX1 gene, which is one that's responsible for the body's organization, specifically in forming lower limbs. In animal studies, when this deletion was introduced to developing birds, their wing buds were noted to take on limb-like structures. People who are affected by Liebenberg Syndrome suffer from three main symptoms: Dysplasia (improper formation) of the bony components of the elbow Abnormal shape of carpal bones Brachydactyly, a symptom where the fingers and toes are shorter than normal.The condition was first described by Dr. F. Liebenberg in 1973 while he followed multiple generations of a South African family, but it has since been noticed in other family lineages across the world.".
- Liebenberg_syndrome omim "186550".
- Liebenberg_syndrome thumbnail Autosomal_dominant.png?width=300.
- Liebenberg_syndrome wikiPageID "37919905".
- Liebenberg_syndrome wikiPageLength "6449".
- Liebenberg_syndrome wikiPageOutDegree "29".
- Liebenberg_syndrome wikiPageRevisionID "700732890".
- Liebenberg_syndrome wikiPageWikiLink Anatomical_terms_of_location.
- Liebenberg_syndrome wikiPageWikiLink Anatomical_terms_of_motion.
- Liebenberg_syndrome wikiPageWikiLink Autosome.
- Liebenberg_syndrome wikiPageWikiLink Brachydactyly.
- Liebenberg_syndrome wikiPageWikiLink Camptodactyly.
- Liebenberg_syndrome wikiPageWikiLink Carpal_bones.
- Liebenberg_syndrome wikiPageWikiLink Category:Genetic_disorders.
- Liebenberg_syndrome wikiPageWikiLink Chromosomal_translocation.
- Liebenberg_syndrome wikiPageWikiLink Deletion_(genetics).
- Liebenberg_syndrome wikiPageWikiLink Dominance_(genetics).
- Liebenberg_syndrome wikiPageWikiLink Dysplasia.
- Liebenberg_syndrome wikiPageWikiLink Enhancer_(genetics).
- Liebenberg_syndrome wikiPageWikiLink H2AFY.
- Liebenberg_syndrome wikiPageWikiLink Homeobox.
- Liebenberg_syndrome wikiPageWikiLink Homologous_chromosome.
- Liebenberg_syndrome wikiPageWikiLink Humerus.
- Liebenberg_syndrome wikiPageWikiLink Olecranon.
- Liebenberg_syndrome wikiPageWikiLink PITX1.
- Liebenberg_syndrome wikiPageWikiLink Phenotype.
- Liebenberg_syndrome wikiPageWikiLink Radius_(bone).
- Liebenberg_syndrome wikiPageWikiLink Transcription_factor.
- Liebenberg_syndrome wikiPageWikiLink Wrist_osteoarthritis.
- Liebenberg_syndrome wikiPageWikiLink Zygosity.
- Liebenberg_syndrome wikiPageWikiLink File:Autosomal_dominant.png.
- Liebenberg_syndrome wikiPageWikiLinkText "Liebenberg syndrome".
- Liebenberg_syndrome name "Liebenberg syndrome".
- Liebenberg_syndrome omim "186550".
- Liebenberg_syndrome wikiPageUsesTemplate Template:Infobox_disease.
- Liebenberg_syndrome wikiPageUsesTemplate Template:Reflist.
- Liebenberg_syndrome subject Category:Genetic_disorders.
- Liebenberg_syndrome hypernym Disease.
- Liebenberg_syndrome type Disease.
- Liebenberg_syndrome type Syndrome.
- Liebenberg_syndrome type Thing.
- Liebenberg_syndrome type Q12136.
- Liebenberg_syndrome comment "Liebenberg Syndrome is a rare autosomal genetic disease that involves a deletion mutation upstream of the PITX1 gene, which is one that's responsible for the body's organization, specifically in forming lower limbs. In animal studies, when this deletion was introduced to developing birds, their wing buds were noted to take on limb-like structures.".
- Liebenberg_syndrome label "Liebenberg syndrome".
- Liebenberg_syndrome sameAs Q6543864.
- Liebenberg_syndrome sameAs Liebenberg-Syndrom.
- Liebenberg_syndrome sameAs m.0p76j04.
- Liebenberg_syndrome sameAs Q6543864.
- Liebenberg_syndrome wasDerivedFrom Liebenberg_syndrome?oldid=700732890.
- Liebenberg_syndrome depiction Autosomal_dominant.png.
- Liebenberg_syndrome isPrimaryTopicOf Liebenberg_syndrome.
- Liebenberg_syndrome name "Liebenberg syndrome".