CMO 1 deficiency (medical condition): A rare genetic, metabolic defect where a deficiency of the enzyme 18-Hydroxylase which results in a reduced amount of aldosterone and salt wasting.
See also:
18-Hydroxylase deficiency:
»Introduction: 18-Hydroxylase deficiency
»Symptoms of 18-Hydroxylase deficiency
These medical condition or symptom topics may be relevant to medical information for CMO 1 deficiency:
CMO 1 deficiency is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that CMO 1 deficiency, or a subtype of CMO 1 deficiency,
affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)
CMO 1 deficiency: Another name for 18-Hydroxylase deficiency (or close medical condition association).
»Introduction: 18-Hydroxylase deficiency
»Symptoms of 18-Hydroxylase deficiency
Some of the symptoms of CMO 1 deficiency incude:
See full list of 7 symptoms of CMO 1 deficiency (18-Hydroxylase deficiency)
Source - NIH
Search to find out more about CMO 1 deficiency:
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