Lipodystrophy, Congenital Generalized D052497

Related MeSH Hierarchy (6)

Diseases [C] » Nutritional and Metabolic Diseases [C18] » Metabolic Diseases » Lipid Metabolism Disorders » Lipid Metabolism, Inborn Errors » Lipodystrophy, Congenital Generalized

Diseases [C] » Skin and Connective Tissue Diseases [C17] » Skin Diseases » Skin Diseases, Metabolic » Lipodystrophy » Lipodystrophy, Congenital Generalized

Diseases [C] » Nutritional and Metabolic Diseases [C18] » Metabolic Diseases » Lipid Metabolism Disorders » Lipodystrophy » Lipodystrophy, Congenital Generalized

Diseases [C] » Nutritional and Metabolic Diseases [C18] » Metabolic Diseases » Metabolism, Inborn Errors » Lipid Metabolism, Inborn Errors » Lipodystrophy, Congenital Generalized

Diseases [C] » Nutritional and Metabolic Diseases [C18] » Metabolic Diseases » Skin Diseases, Metabolic » Lipodystrophy » Lipodystrophy, Congenital Generalized

Description

Congenital disorders, usually autosomal recessive, characterized by severe generalized lack of ADIPOSE TISSUE, extreme INSULIN RESISTANCE, and HYPERTRIGLYCERIDEMIA.   MeSH

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Phase 4 Indicated Drugs (1)

Phase 2 Indicated Drugs (1)


Organization Involved with Phase 4 Indications (1)

Organization Involved with Phase 2 Indications (1)

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