Comprehensive Metabolic Panel (CMP) for Hereditary angioedema with C1Inh deficiency
The comprehensive metabolic panel (cmp) is among the laboratory tests healthcare providers may use to investigate Hereditary angioedema with C1Inh deficiency. Learn what it measures, how to prepare, and what results can tell a provider. Educational content only - not a diagnosis.
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- Sample type
- Blood
- Typical turnaround
- 1-2 business days
- Preparation
- Fasting may be required for 8-12 hours.
Why the comprehensive metabolic panel (cmp) may be ordered for Hereditary angioedema with C1Inh deficiency
Measures 14 substances in the blood to assess kidney and liver function, electrolyte balance, and blood sugar levels.
When evaluating Hereditary angioedema with C1Inh deficiency, a healthcare provider may order the comprehensive metabolic panel (cmp) alongside other tests based on your symptoms, history, and physical exam. Test selection and result interpretation are clinical decisions made by a qualified professional.
Symptoms associated with Hereditary angioedema with C1Inh deficiency
Abdominal pain
An unpleasant sensation characterized by physical discomfort (such as pricking, throbbing, or aching) and perc...
Asthenia
A state characterized by a feeling of weakness and loss of strength leading to a generalized weakness of the b...
Diarrhea
Abnormally increased frequency (usually defined as three or more) loose or watery bowel movements a day....
Facial edema
Information about Facial edema....
Fatigue
A subjective feeling of tiredness characterized by a lack of energy and motivation....
Headache
Cephalgia, or pain sensed in various parts of the head, not confined to the area of distribution of any nerve....
Joint swelling
Information about Joint swelling....
Nausea and vomiting
Nausea is a commonly encountered symptom that has been defined as an unpleasant painless subjective feeling th...
Pain
An unpleasant sensory and emotional experience associated with actual or potential tissue damage, or described...
Paresthesia
Abnormal sensations such as tingling, pricking, or numbness of the skin with no apparent physical cause....
Pharyngeal edema
Abnormal accumulation of fluid leading to swelling of the pharynx....
Skin rash
A red eruption of the skin....
Other tests used to investigate Hereditary angioedema with C1Inh deficiency
CBC with Differential
Measures red blood cells, white blood cells, and platelets to help evaluate overall health and detect disorder...
Urinalysis
Examines urine content to help detect urinary tract infections, kidney disease, and diabetes....
Frequently Asked Questions
Is the comprehensive metabolic panel (cmp) used to investigate Hereditary angioedema with C1Inh deficiency?
Yes - the comprehensive metabolic panel (cmp) is among the tests healthcare providers may consider when evaluating Hereditary angioedema with C1Inh deficiency. Measures 14 substances in the blood to assess kidney and liver function, electrolyte balance, and blood sugar levels. Test selection is a clinical decision made by a qualified professional.
How should I prepare for the comprehensive metabolic panel (cmp)?
Fasting may be required for 8-12 hours.
How long does the comprehensive metabolic panel (cmp) take?
Results for the comprehensive metabolic panel (cmp) are typically available within 1-2 business days depending on the laboratory.
Does this website interpret my comprehensive metabolic panel (cmp) result?
No. SymptomDatabase.com does not interpret laboratory results. Discuss all results with a qualified healthcare provider.