E80 refers to Disorders of porphyrin and bilirubin metabolism, a group of metabolic or genetic disorders affecting how the body processes key molecules like amino acids, carbohydrates, fats, minerals, or enzymes. These may be congenital or acquired, with implications for nutrition, growth, and systemic health.
Diagnosis of Disorders of porphyrin and bilirubin metabolism includes genetic testing, metabolic panels, enzyme assays, stool and urine analysis, sweat chloride test (E84), and imaging. Clinical history and family background play a key role in identifying hereditary metabolic disorders early.
ICD10 code E80 is used across pediatrics, internal medicine, metabolic genetics, endocrinology, and nephrology. It supports documentation of rare diseases, postoperative syndromes, fluid/electrolyte issues, and nutrition-related metabolic dysfunctions.
Q1: What is ICD10 code E80?
A: This code classifies Disorders of porphyrin and bilirubin metabolism, a metabolic or postprocedural condition affecting nutrient or electrolyte balance.
Q2: Are these genetic or acquired?
A: Many (e.g., E70–E80) are inherited, while others like E87 or E89 may be secondary to illness or surgery.
Q3: How are they treated?
A: Treatment varies by disorder—ranging from dietary restrictions to enzyme replacement or fluid/electrolyte rebalancing.
Q4: Who manages these conditions?
A: Geneticists, endocrinologists, metabolic specialists, nephrologists, and pediatricians depending on age and cause.
Q5: Can these be life-threatening?
A: Yes, some are serious without early detection, but many are manageable with proper medical care and monitoring.
ICD10 code E80 enables proper diagnosis and classification of Disorders of porphyrin and bilirubin metabolism. This helps in treatment planning, insurance documentation, and coordinated care—especially in rare metabolic or postoperative endocrine conditions.
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