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DO Term : familial chylomicronemia due to inhibition of lipoprotein lipase activity [DOID:0111419] Disease Ontology
Namespace  disease_ontology Obsolete  false
description  A familial chylomicronemia syndrome characterized by hypertriglyceridemia, chylomicronemia, very low levels of postheparin plasma lipolytic activity, presence in the circulation of a lipoprotein lipase inhibitor, and elevated adipose levels of lipoprotien lipase.
  • synonyms:
  • 118830,
  • OMIM:118830
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Disease

Diseases --> Human genes

Diseases --> Mouse genes

Diseases --> Mouse models

Ontology

Ontology Term --> All ancestors

Ontology Term --> All descendants

Ontology Term --> Direct children

Ontology Term --> Direct parents





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