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- Dunnigan_familial_partial_lipodystrophy abstract "Dunnigan-type familial partial lipodystrophy, abbreviated as (FPLD), is a rare monogenic form of insulin resistance characterized by loss of subcutaneous fat from the extremities, trunk, and gluteal region. FPLD recapitulates the main metabolic attributes of the insulin resistance syndrome, including central obesity, hyperinsulinemia, glucose intolerance and diabetes usually type 2, dyslipidemia, hypertension, and early endpoints of atherosclerosis. It can also result in hepatic steatosis. FPLD results from mutations in LMNA gene, which is the gene that encodes nuclear lamins A and C.".
- Dunnigan_familial_partial_lipodystrophy omim "151660".
- Dunnigan_familial_partial_lipodystrophy wikiPageID "21808773".
- Dunnigan_familial_partial_lipodystrophy wikiPageRevisionID "600839791".
- Dunnigan_familial_partial_lipodystrophy hasPhotoCollection Dunnigan_familial_partial_lipodystrophy.
- Dunnigan_familial_partial_lipodystrophy name "Dunnigan familial partial lipodystrophy".
- Dunnigan_familial_partial_lipodystrophy omim "151660".
- Dunnigan_familial_partial_lipodystrophy subject Category:Conditions_of_the_subcutaneous_fat.
- Dunnigan_familial_partial_lipodystrophy subject Category:Genetic_disorders.
- Dunnigan_familial_partial_lipodystrophy type Abstraction100002137.
- Dunnigan_familial_partial_lipodystrophy type Attribute100024264.
- Dunnigan_familial_partial_lipodystrophy type Condition113920835.
- Dunnigan_familial_partial_lipodystrophy type ConditionsOfTheSubcutaneousFat.
- Dunnigan_familial_partial_lipodystrophy type Disease114070360.
- Dunnigan_familial_partial_lipodystrophy type GeneticDisease114151139.
- Dunnigan_familial_partial_lipodystrophy type GeneticDisorders.
- Dunnigan_familial_partial_lipodystrophy type IllHealth114052046.
- Dunnigan_familial_partial_lipodystrophy type Illness114061805.
- Dunnigan_familial_partial_lipodystrophy type PathologicalState114051917.
- Dunnigan_familial_partial_lipodystrophy type PhysicalCondition114034177.
- Dunnigan_familial_partial_lipodystrophy type State100024720.
- Dunnigan_familial_partial_lipodystrophy type Disease.
- Dunnigan_familial_partial_lipodystrophy type Situation.
- Dunnigan_familial_partial_lipodystrophy comment "Dunnigan-type familial partial lipodystrophy, abbreviated as (FPLD), is a rare monogenic form of insulin resistance characterized by loss of subcutaneous fat from the extremities, trunk, and gluteal region. FPLD recapitulates the main metabolic attributes of the insulin resistance syndrome, including central obesity, hyperinsulinemia, glucose intolerance and diabetes usually type 2, dyslipidemia, hypertension, and early endpoints of atherosclerosis. It can also result in hepatic steatosis.".
- Dunnigan_familial_partial_lipodystrophy label "Dunnigan familial partial lipodystrophy".
- Dunnigan_familial_partial_lipodystrophy sameAs m.05pbgr6.
- Dunnigan_familial_partial_lipodystrophy sameAs Q5315596.
- Dunnigan_familial_partial_lipodystrophy sameAs Q5315596.
- Dunnigan_familial_partial_lipodystrophy sameAs Dunnigan_familial_partial_lipodystrophy.
- Dunnigan_familial_partial_lipodystrophy wasDerivedFrom Dunnigan_familial_partial_lipodystrophy?oldid=600839791.
- Dunnigan_familial_partial_lipodystrophy isPrimaryTopicOf Dunnigan_familial_partial_lipodystrophy.
- Dunnigan_familial_partial_lipodystrophy name "Dunnigan familial partial lipodystrophy".