Hurler syndrome and ICD-10 Chapter IV: Endocrine, nutritional and metabolic diseases

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

Difference between Hurler syndrome and ICD-10 Chapter IV: Endocrine, nutritional and metabolic diseases

Hurler syndrome vs. ICD-10 Chapter IV: Endocrine, nutritional and metabolic diseases

Hurler syndrome is also known as mucopolysaccharidosis type IH (MPS IH), Hurler's disease, and formerly gargoylism. This is an overview about the chapter IV (also called chapter E) of the International Statistical Classification of Diseases and Related Health Problems 10th Revision (ICD-10).

Similarities between Hurler syndrome and ICD-10 Chapter IV: Endocrine, nutritional and metabolic diseases

Hurler syndrome and ICD-10 Chapter IV: Endocrine, nutritional and metabolic diseases have 6 things in common (in Unionpedia): Cornea, Genetic disorder, Glycosaminoglycan, Hunter syndrome, Lysosome, Mucopolysaccharidosis.

Cornea

The cornea is the transparent front part of the eye that covers the iris, pupil, and anterior chamber.

Cornea and Hurler syndrome · Cornea and ICD-10 Chapter IV: Endocrine, nutritional and metabolic diseases · See more »

Genetic disorder

A genetic disorder is a genetic problem caused by one or more abnormalities in the genome.

Genetic disorder and Hurler syndrome · Genetic disorder and ICD-10 Chapter IV: Endocrine, nutritional and metabolic diseases · See more »

Glycosaminoglycan

Glycosaminoglycans (GAGs) or mucopolysaccharides are long unbranched polysaccharides consisting of a repeating disaccharide unit.

Glycosaminoglycan and Hurler syndrome · Glycosaminoglycan and ICD-10 Chapter IV: Endocrine, nutritional and metabolic diseases · See more »

Hunter syndrome

Hunter syndrome, or mucopolysaccharidosis type II (MPS II), is a lysosomal storage disease caused by a deficiency of the lysosomal enzyme iduronate-2-sulfatase (I2S).

Hunter syndrome and Hurler syndrome · Hunter syndrome and ICD-10 Chapter IV: Endocrine, nutritional and metabolic diseases · See more »

Lysosome

A lysosome is a membrane-bound organelle found in nearly all animal cells.

Hurler syndrome and Lysosome · ICD-10 Chapter IV: Endocrine, nutritional and metabolic diseases and Lysosome · See more »

Mucopolysaccharidosis

Mucopolysaccharidoses are a group of metabolic disorders caused by the absence or malfunctioning of lysosomal enzymes needed to break down molecules called glycosaminoglycans.

Hurler syndrome and Mucopolysaccharidosis · ICD-10 Chapter IV: Endocrine, nutritional and metabolic diseases and Mucopolysaccharidosis · See more »

The list above answers the following questions

What Hurler syndrome and ICD-10 Chapter IV: Endocrine, nutritional and metabolic diseases have in common
What are the similarities between Hurler syndrome and ICD-10 Chapter IV: Endocrine, nutritional and metabolic diseases

Hurler syndrome and ICD-10 Chapter IV: Endocrine, nutritional and metabolic diseases Comparison

Hurler syndrome has 55 relations, while ICD-10 Chapter IV: Endocrine, nutritional and metabolic diseases has 388. As they have in common 6, the Jaccard index is 1.35% = 6 / (55 + 388).

References

This article shows the relationship between Hurler syndrome and ICD-10 Chapter IV: Endocrine, nutritional and metabolic diseases. To access each article from which the information was extracted, please visit:

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