CPO deficiency

Introduction: CPO deficiency

Description of CPO deficiency

CPO deficiency (medical condition): An inherited metabolic disorder involving a deficiency of...more »

See also:

Dobriner syndrome:
  »Introduction: Dobriner syndrome
  »Symptoms of Dobriner syndrome

CPO deficiency: Related Topics

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

• Deficiency
• Deficiency disease

CPO deficiency: Rare Disease

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

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

CPO deficiency as a Disease

CPO deficiency: Another name for Dobriner syndrome (or close medical condition association).
  »Introduction: Dobriner syndrome
  »Symptoms of Dobriner syndrome

CPO deficiency: Related Diseases

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

• Congenital conditions - metabolic disorders
• Congenital conditions
• Metabolic conditions

Symptoms of CPO deficiency (Dobriner syndrome)

Some of the symptoms of CPO deficiency incude:

• Abdominal pain
• Neurological manifestations
• Psychiatric manifestations
• Hepatic insufficiency
• Photosensitivity

See full list of 19 symptoms of CPO deficiency (Dobriner syndrome)

CPO deficiency: Related Disease Topics

These medical disease topics may be related to CPO deficiency:

• abdominal pain
• arm pain
• constipation
• increased heart rate
• leg pain
• urinary retention
• vomiting
• psychosis
• hallucinations
• confusion

Terms associated with CPO deficiency:

Terms Similar to CPO deficiency:

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

Source - NIH

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