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Problem
Congenital disorders of lipid metabolism
Experimental visualization of narrower problems
Other Names:
Glycolipidosis disorders
Inherited metabolic diseases producing storage of sphingolipids
Sphingolipidoses
Disorders of sphingolipid metabolism
Sphingolipidosis
Familial lipid storage disorders
Neurolipidoses
Broader Problems:
Lipid storage disorder
Lysosomal storage diseases
Hereditary metabolic diseases
Hereditary disorders of the central nervous system
Lipid metabolic diseases
Narrower Problems:
Fabry disease
Farber disease
Gangliosidosis
Sandhoff disease
Krabbe's disease
Gaucher's disease
Tay-Sachs disease
X-linked ichthyosis
Niemann-Pick disease
Cholesterol storage diseases
Metachromatic leucodystrophy
Multiple sulphatase deficiency
Pseudo arylsulphatase deficiency
Aggravates:
Coronary heart disease
Values:
Disorder
References:
Salvayre, R, et al: Lipid Storage Disorders: biological and medical aspects
Subject(s):
Biosciences
→
Biochemistry
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Biosciences
→
Genetics
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Fundamental Sciences
→
Organic chemical compounds
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Industry
→
Production
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Medicine
→
Pathology
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Society
→
Family
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Transportation, Telecommunications
→
Storage
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Related UN Sustainable Development Goals:
Problem Type:
E: Emanations of other problems
Date of last update
23.04.2019 – 11:27 CEST