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CPS1 Deficiency (medical condition): A very rare inherited urea cycle disorder where the lack of...more »
These medical condition or symptom topics may be relevant to medical information for CPS1 Deficiency:
CPS1 Deficiency is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that CPS1 Deficiency, or a subtype of CPS1 Deficiency,
affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)
CPS1 Deficiency: Another name for Carbamoyl-phosphate synthase 1 deficiency (or close medical condition association).
»Introduction: Carbamoyl-phosphate synthase 1 deficiency
»Symptoms of Carbamoyl-phosphate synthase 1 deficiency
CPS1 Deficiency: CPS1 Deficiency is listed as a type of (or associated with) the following medical conditions in our database:
Some of the symptoms of CPS1 Deficiency incude:
These medical disease topics may be related to CPS1 Deficiency:
Source - NIH
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