ICD-10 Code | E72.3 |
Description | Disorders of lysine and hydroxylysine metabolism |
Hierarchy | |
Billable status | ICD-10-CM Billable code |
Type 1transitory endocrine and metabolic disorders specific to newborn (P70-P74)
Type 1androgen insensitivity syndrome (E34.5-)
Type 1congenital adrenal hyperplasia (E25.0)
Type 1hemolytic anemias attributable to enzyme disorders (D55.-)
Type 1Marfan syndrome (Q87.4-)
Type 15-alpha-reductase deficiency (E29.1)
Type 2Ehlers-Danlos syndromes (Q79.6-)
Type 1disorders of:
Type 1aromatic amino-acid metabolism (E70.-)
Type 1branched-chain amino-acid metabolism (E71.0-E71.2)
Type 1fatty-acid metabolism (E71.3)
Type 1purine and pyrimidine metabolism (E79.-)
Type 1gout (M1A.-, M10.-)
Type 1glutaric aciduria type II (E71.313)
Type 1Refsum's disease (G60.1)
Type 1Zellweger syndrome (E71.510)