ECI Qualifying Diagnosis Search

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Diagnosis Results

Qualifying Diagnosis Codes have the following notation: < Q >

• • E00 Congenital iodine-deficiency syndrome
    • E00.0 <Q> Congenital iodine-deficiency syndrome, neurological type
    • E00.1 <Q> Congenital iodine-deficiency syndrome, myxedematous type
    • E00.2 <Q> Congenital iodine-deficiency syndrome, mixed type
    • E00.9 <Q> Congenital iodine-deficiency syndrome, unspecified
  • E03 Other hypothyroidism
    • E03.0 <Q> Congenital hypothyroidism with diffuse goiter
    • E03.1 <Q> Congenital hypothyroidism without goiter
• • E22 Hyperfunction of pituitary gland
    • E22.0 <Q> Acromegaly and pituitary gigantism
  • E23 Hypofunction and other disorders of the pituitary gland
    • E23.0 <Q> Hypopituitarism
  • E26 Hyperaldosteronism
    • E26.8 Other hyperaldosteronism
  • E34 Other endocrine disorders
    • E34.8 <Q> Other specified endocrine disorders
• • E70 Disorders of aromatic amino-acid metabolism
    • E70.0 <Q> Classical phenylketonuria
    • E70.2 Disorders of tyrosine metabolism
  • E71 Disorders of branched-chain amino-acid metabolism and fatty-acid metabolism
    • E71.0 <Q> Maple-syrup-urine disease
    • E71.1 Other disorders of branched-chain amino-acid metabolism
    • E71.3 Disorders of fatty-acid metabolism
    • E71.5 Peroxisomal disorders
  • E72 Other disorders of amino-acid metabolism
    • E72.0 Disorders of amino-acid transport
    • E72.1 Disorders of sulfur-bearing amino-acid metabolism
    • E72.2 Disorders of urea cycle metabolism
    • E72.3 <Q> Disorders of lysine and hydroxylysine metabolism
    • E72.5 Disorders of glycine metabolism
  • E74 Other disorders of carbohydrate metabolism
    • E74.0 Glycogen storage disease
    • E74.2 Disorders of galactose metabolism
  • E75 Disorders of sphingolipid metabolism and other lipid storage disorders
    • E75.0 GM2 gangliosidosis
    • E75.1 Other and unspecified gangliosidosis
    • E75.2 Other sphingolipidosis
    • E75.3 <Q> Sphingolipidosis, unspecified
    • E75.4 <Q> Neuronal ceroid lipofuscinosis
    • E75.5 <Q> Other lipid storage disorders
  • E76 Disorders of glycosaminoglycan metabolism
    • E76.3 <Q> Mucopolysaccharidosis, unspecified
  • E77 Disorders of glycoprotein metabolism
    • E77.0 <Q> Defects in post-translational modification of lysosomal enzymes
    • E77.1 <Q> Defects in glycoprotein degradation
  • E78 Disorders of lipoprotein metabolism and other lipidemias
    • E78.7 Disorders of bile acid and cholesterol metabolism
  • E79 Disorders of purine and pyrimidine metabolism
    • E79.1 <Q> Lesch-Nyhan syndrome
  • E83 Disorders of mineral metabolism
    • E83.0 Disorders of copper metabolism