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- MELAS_syndrome abstract "Mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes – abbreviated to MELAS – is one of the family of mitochondrial cytopathies, which also include MERRF, and Leber's hereditary optic neuropathy. It was first characterized under this name in 1984. A feature of these diseases is that they are caused by defects in the mitochondrial genome which is inherited purely from the female parent. However, it is important to know that some of the proteins essential to normal mitochondrial function are produced by the nuclear genome, and are subsequently transported to the mitochondria for use. As such, mutations in these proteins can result in mitochondrial disorders, but can be inherited from both male and female parent in the typical fashion. The disease can manifest in both sexes.".
- MELAS_syndrome diseasesdb "8254".
- MELAS_syndrome emedicineSubject "ped".
- MELAS_syndrome emedicineTopic "1406".
- MELAS_syndrome icd10 "G31.8".
- MELAS_syndrome icd9 "277.87".
- MELAS_syndrome meshId "D017241".
- MELAS_syndrome omim "540000".
- MELAS_syndrome thumbnail A_computed_tomography_brain_scan_showing_bilateral_basal_ganglia_calcification.jpg?width=300.
- MELAS_syndrome wikiPageID "3713191".
- MELAS_syndrome wikiPageRevisionID "602178483".
- MELAS_syndrome caption "Basal ganglia calcification, cerebellar atrophy, increased lactate; a CT image of a person diagnosed with MELAS".
- MELAS_syndrome diseasesdb "8254".
- MELAS_syndrome emedicinesubj "ped".
- MELAS_syndrome emedicinetopic "1406".
- MELAS_syndrome hasPhotoCollection MELAS_syndrome.
- MELAS_syndrome icd "277.87".
- MELAS_syndrome icd "G31.8".
- MELAS_syndrome meshid "D017241".
- MELAS_syndrome name "Mitochondrial myopathy, encephalomyopathy, lactic acidosis, and stroke-like episodes".
- MELAS_syndrome omim "540000".
- MELAS_syndrome subject Category:Genodermatoses.
- MELAS_syndrome subject Category:Mitochondrial_diseases.
- MELAS_syndrome type Abstraction100002137.
- MELAS_syndrome type Attribute100024264.
- MELAS_syndrome type Condition113920835.
- MELAS_syndrome type Disease114070360.
- MELAS_syndrome type IllHealth114052046.
- MELAS_syndrome type Illness114061805.
- MELAS_syndrome type PathologicalState114051917.
- MELAS_syndrome type PhysicalCondition114034177.
- MELAS_syndrome type State100024720.
- MELAS_syndrome type Disease.
- MELAS_syndrome type Situation.
- MELAS_syndrome comment "Mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes – abbreviated to MELAS – is one of the family of mitochondrial cytopathies, which also include MERRF, and Leber's hereditary optic neuropathy. It was first characterized under this name in 1984. A feature of these diseases is that they are caused by defects in the mitochondrial genome which is inherited purely from the female parent.".
- MELAS_syndrome label "MELAS syndrome".
- MELAS_syndrome label "MELAS".
- MELAS_syndrome label "Miopatia mitocondriale con encefalopatia, acidosi lattica ed episodi tipo ictus".
- MELAS_syndrome label "Syndrome MELAS".
- MELAS_syndrome label "Síndrome MELAS".
- MELAS_syndrome label "Zespół MELAS".
- MELAS_syndrome label "Синдром MELAS".
- MELAS_syndrome sameAs Síndrome_MELAS.
- MELAS_syndrome sameAs Syndrome_MELAS.
- MELAS_syndrome sameAs Miopatia_mitocondriale_con_encefalopatia,_acidosi_lattica_ed_episodi_tipo_ictus.
- MELAS_syndrome sameAs MELAS.
- MELAS_syndrome sameAs Zespół_MELAS.
- MELAS_syndrome sameAs m.09wr_0.
- MELAS_syndrome sameAs Q2666433.
- MELAS_syndrome sameAs Q2666433.
- MELAS_syndrome sameAs MELAS_syndrome.
- MELAS_syndrome wasDerivedFrom MELAS_syndrome?oldid=602178483.
- MELAS_syndrome depiction A_computed_tomography_brain_scan_showing_bilateral_basal_ganglia_calcification.jpg.
- MELAS_syndrome isPrimaryTopicOf MELAS_syndrome.
- MELAS_syndrome name "Mitochondrial myopathy, encephalomyopathy, lactic acidosis, and stroke-like episodes".
