CPS1 Deficiency

Introduction: CPS1 Deficiency

Description of CPS1 Deficiency

CPS1 Deficiency (medical condition): A very rare inherited urea cycle disorder where the lack of...more »

CPS1 Deficiency: Related Topics

These medical condition or symptom topics may be relevant to medical information for CPS1 Deficiency:

CPS1 Deficiency: Rare Disease

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

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 as a Disease

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: Related Diseases

CPS1 Deficiency: CPS1 Deficiency is listed as a type of (or associated with) the following medical conditions in our database:

Symptoms of CPS1 Deficiency (Carbamoyl-phosphate synthase 1 deficiency)

Some of the symptoms of CPS1 Deficiency incude:

See full list of 15 symptoms of CPS1 Deficiency (Carbamoyl-phosphate synthase 1 deficiency)

CPS1 Deficiency: Related Disease Topics

These medical disease topics may be related to CPS1 Deficiency:

Terms associated with CPS1 Deficiency:

Terms Similar to CPS1 Deficiency:

Source - NIH

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