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Dictionary » Glycinemia, ketotic

Glycinemia, ketotic

Introduction: Glycinemia, ketotic

Description of Glycinemia, ketotic

Glycinemia, ketotic (medical condition): An inherited genetic disorder where the body is incapable of processing some...more »

See also:

Acidemia, propionic:
  »Introduction: Acidemia, propionic
  »Symptoms of Acidemia, propionic

Glycinemia, ketotic: Related Topics

These medical condition or symptom topics may be relevant to medical information for Glycinemia, ketotic:

Glycinemia, ketotic: Rare Disease

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

Glycinemia, ketotic is listed as a "rare disease" by the Office of Rare Diseases (ORD) of the National Institutes of Health (NIH). This means that Glycinemia, ketotic, or a subtype of Glycinemia, ketotic, affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)


Ophanet, a consortium of European partners, currently defines a condition rare when if affects 1 person per 2,000. They list Glycinemia, ketotic as a "rare disease".

Source - Orphanet

Glycinemia, ketotic as a Disease

Glycinemia, ketotic: Another name for Acidemia, propionic (or close medical condition association).
  »Introduction: Acidemia, propionic
  »Symptoms of Acidemia, propionic

Glycinemia, ketotic: Related Diseases

Glycinemia, ketotic: Glycinemia, ketotic is listed as a type of (or associated with) the following medical conditions in our database:

Symptoms of Glycinemia, ketotic (Acidemia, propionic)

Some of the symptoms of Glycinemia, ketotic incude:

Terms associated with Glycinemia, ketotic:

Terms Similar to Glycinemia, ketotic:

Source - NIH

Interesting Medical Articles:

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