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Hepatic porphyria and ICD-10 Chapter IV: Endocrine, nutritional and metabolic diseases

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

Difference between Hepatic porphyria and ICD-10 Chapter IV: Endocrine, nutritional and metabolic diseases

Hepatic porphyria vs. ICD-10 Chapter IV: Endocrine, nutritional and metabolic diseases

Hepatic porphyrias is a form of porphyria in which the enzyme deficiency occurs in the liver. 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 Hepatic porphyria and ICD-10 Chapter IV: Endocrine, nutritional and metabolic diseases

Hepatic porphyria and ICD-10 Chapter IV: Endocrine, nutritional and metabolic diseases have 7 things in common (in Unionpedia): Acute intermittent porphyria, Erythropoietic porphyria, Hepatoerythropoietic porphyria, Hereditary coproporphyria, Porphyria, Porphyria cutanea tarda, Variegate porphyria.

Acute intermittent porphyria

Acute intermittent porphyria (AIP) is a genetic metabolic disorder affecting the production of heme, the oxygen-binding prosthetic group of hemoglobin.

Acute intermittent porphyria and Hepatic porphyria · Acute intermittent porphyria and ICD-10 Chapter IV: Endocrine, nutritional and metabolic diseases · See more »

Erythropoietic porphyria

Erythropoietic porphyria is a type of porphyria associated with erythropoietic cells.

Erythropoietic porphyria and Hepatic porphyria · Erythropoietic porphyria and ICD-10 Chapter IV: Endocrine, nutritional and metabolic diseases · See more »

Hepatoerythropoietic porphyria

Hepatoerythropoietic porphyria is a very rare form of hepatic porphyria caused by a disorder in both genes which code Uroporphyrinogen III decarboxylase (UROD).

Hepatic porphyria and Hepatoerythropoietic porphyria · Hepatoerythropoietic porphyria and ICD-10 Chapter IV: Endocrine, nutritional and metabolic diseases · See more »

Hereditary coproporphyria

Hereditary coproporphyria (HCP) is a disorder of heme biosynthesis, classified as an acute hepatic porphyria.

Hepatic porphyria and Hereditary coproporphyria · Hereditary coproporphyria and ICD-10 Chapter IV: Endocrine, nutritional and metabolic diseases · See more »

Porphyria

Porphyria is a group of diseases in which substances called porphyrins build up, negatively affecting the skin or nervous system.

Hepatic porphyria and Porphyria · ICD-10 Chapter IV: Endocrine, nutritional and metabolic diseases and Porphyria · See more »

Porphyria cutanea tarda

Porphyria cutanea tarda (PCT) is the most common subtype of porphyria.

Hepatic porphyria and Porphyria cutanea tarda · ICD-10 Chapter IV: Endocrine, nutritional and metabolic diseases and Porphyria cutanea tarda · See more »

Variegate porphyria

Variegate porphyria, also known by several other names, is an autosomal dominant porphyria that can have acute (severe but usually not long-lasting) symptoms along with symptoms that affect the skin.

Hepatic porphyria and Variegate porphyria · ICD-10 Chapter IV: Endocrine, nutritional and metabolic diseases and Variegate porphyria · See more »

The list above answers the following questions

Hepatic porphyria and ICD-10 Chapter IV: Endocrine, nutritional and metabolic diseases Comparison

Hepatic porphyria has 8 relations, while ICD-10 Chapter IV: Endocrine, nutritional and metabolic diseases has 388. As they have in common 7, the Jaccard index is 1.77% = 7 / (8 + 388).

References

This article shows the relationship between Hepatic porphyria 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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