Carnitine palmitoyltransferase II deficiency and Skeletal muscle

Shortcuts: Differences, Similarities, Jaccard Similarity Coefficient, References.

Difference between Carnitine palmitoyltransferase II deficiency and Skeletal muscle

Carnitine palmitoyltransferase II deficiency vs. Skeletal muscle

Carnitine palmitoyltransferase II deficiency (CPT-II) is an autosomal recessively inherited genetic metabolic disorder characterized by an enzymatic defect that prevents long-chain fatty acids from being transported into the mitochondria for utilization as an energy source. Skeletal muscle is one of three major muscle types, the others being cardiac muscle and smooth muscle.

Similarities between Carnitine palmitoyltransferase II deficiency and Skeletal muscle

Carnitine palmitoyltransferase II deficiency and Skeletal muscle have 2 things in common (in Unionpedia): Mitochondrion, Myopathy.

Mitochondrion

The mitochondrion (plural mitochondria) is a double-membrane-bound organelle found in most eukaryotic organisms.

Carnitine palmitoyltransferase II deficiency and Mitochondrion · Mitochondrion and Skeletal muscle · See more »

Myopathy

Myopathy is a disease of the muscle in which the muscle fibers do not function properly.

Carnitine palmitoyltransferase II deficiency and Myopathy · Myopathy and Skeletal muscle · See more »

The list above answers the following questions

What Carnitine palmitoyltransferase II deficiency and Skeletal muscle have in common
What are the similarities between Carnitine palmitoyltransferase II deficiency and Skeletal muscle

Carnitine palmitoyltransferase II deficiency and Skeletal muscle Comparison

Carnitine palmitoyltransferase II deficiency has 41 relations, while Skeletal muscle has 89. As they have in common 2, the Jaccard index is 1.54% = 2 / (41 + 89).

References

This article shows the relationship between Carnitine palmitoyltransferase II deficiency and Skeletal muscle. To access each article from which the information was extracted, please visit:

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