Coproporphyria

Introduction: Coproporphyria

Description of Coproporphyria

Coproporphyria (medical condition): An inherited disorder that affects the nervous system and sometimes the skin. It...more »

See also:

Porphyria, hereditary coproporphyria:
  »Introduction: Porphyria, hereditary coproporphyria
  »Symptoms of Porphyria, hereditary coproporphyria

Coproporphyria: Inherited disorder of the metabolic system where excess porphyrins are excreted in the faeces.

Coproporphyria: Related Topics

These medical condition or symptom topics may be relevant to medical information for Coproporphyria:

• MIM
• Urine
• Urine symptoms (630 causes)
• Porphyria

Coproporphyria: Rare Disease

Office of Rare Diseases (ORD) of the National Institutes of Health (NIH)

Coproporphyria is listed as a "rare disease" by the Office of Rare Diseases (ORD) of the National Institutes of Health (NIH). This means that Coproporphyria, or a subtype of Coproporphyria, affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)

Coproporphyria as a Disease

Coproporphyria: Another name for Porphyria, hereditary coproporphyria (or close medical condition association).
  »Introduction: Porphyria, hereditary coproporphyria
  »Symptoms of Porphyria, hereditary coproporphyria

Coproporphyria: Related Diseases

Coproporphyria: Coproporphyria is listed as a type of (or associated with) the following medical conditions in our database:

• Genetic conditions
• Metabolic conditions
• Skin conditions
• Nervous system conditions
• Congenital conditions - metabolic disorders
• Congenital conditions

Symptoms of Coproporphyria (Porphyria, hereditary coproporphyria)

Some of the symptoms of Coproporphyria incude:

• Stomach pain
• Dark urine
• Arm pain
• Arm numbness
• Arm tingling

See full list of 27 symptoms of Coproporphyria (Porphyria, hereditary coproporphyria)

Terms associated with Coproporphyria:

Terms Similar to Coproporphyria:

• CPO deficiency
• CPRO deficiency
• CPX deficiency
• Coproporphyrinogen oxidase deficiency
• HCP
• Hereditary coproporphyria (subtype)

Source - NIH

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