Early Childhood Intervention Services

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ECI Qualifying Diagnosis Search


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To search for medically qualifying diagnoses enter the name of the condition or diagnosis code in the search box below and hit 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