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- Berdon_syndrome abstract "Berdon syndrome, also called Megacystis-microcolon-intestinal hypoperistalsis syndrome (MMIH syndrome), is an autosomal recessive genetic disorder affecting newborns. It is more prevalent in females, and is characterized by constipation and urinary retention, microcolon, giant bladder (megacystis), intestinal hypoperistalis, hydronephrosis, and dilated small bowel. The pathological findings consist of an abundance of ganglion cells in both dilated and narrow areas of the intestine. It is a familial disturbance of unknown aetiology. Walter Berdon et al. in 1976 first described the condition in five female infants, two of whom were sisters. All had marked dilatation of the bladder and some had hydronephrosis and the external appearance of prune belly. The infants also had microcolon and dilated small intestines.".
- Berdon_syndrome diseasesdb "32131".
- Berdon_syndrome omim "249210".
- Berdon_syndrome thumbnail Autorecessive.svg?width=300.
- Berdon_syndrome wikiPageExternalLink displaycommon.cfm?an=1&subarticlenbr=54.
- Berdon_syndrome wikiPageID "1181346".
- Berdon_syndrome wikiPageRevisionID "474791831".
- Berdon_syndrome diseasesdb "32131".
- Berdon_syndrome hasPhotoCollection Berdon_syndrome.
- Berdon_syndrome name "Berdon syndrome".
- Berdon_syndrome omim "249210".
- Berdon_syndrome subject Category:Autosomal_recessive_disorders.
- Berdon_syndrome subject Category:Genetic_disorders_with_OMIM_but_no_gene.
- Berdon_syndrome subject Category:Pediatrics.
- Berdon_syndrome subject Category:Syndromes.
- Berdon_syndrome type Abstraction100002137.
- Berdon_syndrome type Attribute100024264.
- Berdon_syndrome type AutosomalRecessiveDisorders.
- Berdon_syndrome type Cognition100023271.
- Berdon_syndrome type Complex105870365.
- Berdon_syndrome type Concept105835747.
- Berdon_syndrome type Condition113920835.
- Berdon_syndrome type Content105809192.
- Berdon_syndrome type Disease114070360.
- Berdon_syndrome type Disorder114052403.
- Berdon_syndrome type GeneticDisease114151139.
- Berdon_syndrome type GeneticDisordersWithOMIMButNoGene.
- Berdon_syndrome type Idea105833840.
- Berdon_syndrome type IllHealth114052046.
- Berdon_syndrome type Illness114061805.
- Berdon_syndrome type PathologicalState114051917.
- Berdon_syndrome type PhysicalCondition114034177.
- Berdon_syndrome type PsychologicalFeature100023100.
- Berdon_syndrome type State100024720.
- Berdon_syndrome type Syndrome105870790.
- Berdon_syndrome type Syndromes.
- Berdon_syndrome type Whole105869584.
- Berdon_syndrome type Disease.
- Berdon_syndrome type AilmentCondition.
- Berdon_syndrome type Situation.
- Berdon_syndrome comment "Berdon syndrome, also called Megacystis-microcolon-intestinal hypoperistalsis syndrome (MMIH syndrome), is an autosomal recessive genetic disorder affecting newborns. It is more prevalent in females, and is characterized by constipation and urinary retention, microcolon, giant bladder (megacystis), intestinal hypoperistalis, hydronephrosis, and dilated small bowel. The pathological findings consist of an abundance of ganglion cells in both dilated and narrow areas of the intestine.".
- Berdon_syndrome label "Berdon syndrome".
- Berdon_syndrome label "متلازمة بيردون".
- Berdon_syndrome sameAs m.04f2qk.
- Berdon_syndrome sameAs Q4891136.
- Berdon_syndrome sameAs Q4891136.
- Berdon_syndrome sameAs Berdon_syndrome.
- Berdon_syndrome wasDerivedFrom Berdon_syndrome?oldid=474791831.
- Berdon_syndrome depiction Autorecessive.svg.
- Berdon_syndrome isPrimaryTopicOf Berdon_syndrome.
- Berdon_syndrome name "Berdon syndrome".