Other disturbances of straight-chain amino-acid metabolism
2015
Billable Thru Sept 30/2015
Non-Billable On/After Oct 1/2015
ICD-9-CM 270.7 is a billable medical code that can be used to indicate a diagnosis on a reimbursement claim, however, 270.7 should only be used for claims with a date of service on or before September 30, 2015. For claims with a date of service on or after October 1, 2015, use an equivalent ICD-10-CM code (or codes).
2015/16 ICD-10-CM E72.3 Disorders of lysine and hydroxylysine metabolism
Or:
2015/16 ICD-10-CM E72.8 Other specified disorders of amino-acid metabolism
Approximate Synonyms
3-Phosphoglycerate dehydrogenase deficiency
Adenosylcobalamin and methylcobalamin synthesis defect
Complete deficiency of methylmalonyl-CoA mutase
Disorder of glutamine metabolism
Disorder of glycine metabolism
Disorder of lysine and hydroxylysine metabolism
Disorder of lysine AND/OR hydroxylysine metabolism
Disorder of serine metabolism
Disorder of threonine metabolism
Glucoglycinuria
Glutaric acidemia type 1
Glutaric acidemia, type 1
Glutaric aciduria, type 1
Glutaryl-CoA dehydrogenase deficiency
Glycine dehydrogenase deficiency
Glycine metabolism disorder
Hyperglycinemia
Hyperglycinemia, non ketotic
Hyperlysinemia
Impaired fasting glycaemia
Intolerance, lysinuric protein
Lysine and hydroxylysine metabolism disorder
Lysine intolerance
Lysinuric protein intolerance
Lysinuric protein intolerance, type 1
Lysinuric protein intolerance, type 2
Methylmalonic acidemia
Non ketotic hyperglycinemia
Non-ketotic hyperglycinemia
Non-ketotic hyperglycinemia H protein deficiency
Non-ketotic hyperglycinemia L protein deficiency
Periodic hyperlysinemia
Periodic hyperlysinemia with hyperammonemia
Persistent hyperlysinemia
Pipecolic acidemia
Saccharopinuria
Transient neonatal hyperglycinemia
Clinical Information
Autosomal recessive metabolic disorder caused by deficiencies in the mitochondrial glycine cleavage system; an enzyme system with four components: p-, t-, h-, and l-proteins; deficiency of the p-protein is the most prevalent form; clinical features include seizures, hypotonia, apnea, and coma; when the illness presents in childhood there tends to be an associated progressive dementia accompanied by extrapyramidal signs
Applies To
Glucoglycinuria
Glycinemia (with methylmalonic acidemia)
Hyperglycinemia
Hyperlysinemia
Pipecolic acidemia
Saccharopinuria
Other disturbances of metabolism of glycine, threonine, serine, glutamine, and lysine