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- GM2-gangliosidosis,_AB_variant abstract "GM2-gangliosidosis, AB variant is a rare, autosomal recessive metabolic disorder that causes progressive destruction of nerve cells in the brain and spinal cord. It has a similar pathology to Sandhoff disease and Tay-Sachs disease. The three diseases are classified together as the GM2 gangliosidoses, because each disease represents a distinct molecular point of failure in the activation of the same enzyme, beta-hexosaminidase. AB variant is caused by a failure in the gene that makes an enzyme cofactor for beta-hexosaminidase, called the GM2 activator.".
- GM2-gangliosidosis,_AB_variant diseasesdb "32644".
- GM2-gangliosidosis,_AB_variant emedicineSubject "ped".
- GM2-gangliosidosis,_AB_variant emedicineTopic "3016".
- GM2-gangliosidosis,_AB_variant meshId "D049290".
- GM2-gangliosidosis,_AB_variant omim "272750".
- GM2-gangliosidosis,_AB_variant wikiPageID "2525674".
- GM2-gangliosidosis,_AB_variant wikiPageRevisionID "591480716".
- GM2-gangliosidosis,_AB_variant diseasesdb "32644".
- GM2-gangliosidosis,_AB_variant emedicinesubj "ped".
- GM2-gangliosidosis,_AB_variant emedicinetopic "3016".
- GM2-gangliosidosis,_AB_variant hasPhotoCollection GM2-gangliosidosis,_AB_variant.
- GM2-gangliosidosis,_AB_variant meshid "D049290".
- GM2-gangliosidosis,_AB_variant name "GM2-gangliosidosis, AB variant".
- GM2-gangliosidosis,_AB_variant omim "272750".
- GM2-gangliosidosis,_AB_variant wordnet_type synset-disease-noun-1.
- GM2-gangliosidosis,_AB_variant subject Category:Autosomal_recessive_disorders.
- GM2-gangliosidosis,_AB_variant subject Category:Lipid_storage_disorders.
- GM2-gangliosidosis,_AB_variant subject Category:Rare_diseases.
- GM2-gangliosidosis,_AB_variant type Disease.
- GM2-gangliosidosis,_AB_variant type AilmentCondition.
- GM2-gangliosidosis,_AB_variant type Situation.
- GM2-gangliosidosis,_AB_variant comment "GM2-gangliosidosis, AB variant is a rare, autosomal recessive metabolic disorder that causes progressive destruction of nerve cells in the brain and spinal cord. It has a similar pathology to Sandhoff disease and Tay-Sachs disease. The three diseases are classified together as the GM2 gangliosidoses, because each disease represents a distinct molecular point of failure in the activation of the same enzyme, beta-hexosaminidase.".
- GM2-gangliosidosis,_AB_variant label "GM2-gangliosidosis, AB variant".
- GM2-gangliosidosis,_AB_variant sameAs m.07kyb7.
- GM2-gangliosidosis,_AB_variant sameAs Q5513688.
- GM2-gangliosidosis,_AB_variant sameAs Q5513688.
- GM2-gangliosidosis,_AB_variant sameAs 2509.
- GM2-gangliosidosis,_AB_variant wasDerivedFrom GM2-gangliosidosis,_AB_variant?oldid=591480716.
- GM2-gangliosidosis,_AB_variant isPrimaryTopicOf GM2-gangliosidosis,_AB_variant.
- GM2-gangliosidosis,_AB_variant name "GM2-gangliosidosis, AB variant".