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Early Intervention Colorado maintains this database by working with a panel of physicians to establish physical or mental conditions that have a high probability of resulting in a significant level of developmental delay. The links below offer you options for viewing the conditions reviewed and approved by the panel.

To review the list of conditions reviewed to date, click here. To submit a condition that has not been reviewed to date contact Beth Cole at 303-866-5017 or Beth.Cole@state.co.us.

Established conditions are listed alphabetically. Use the search form below or click the letter of the alphabet that is the first letter of the diagnosis.


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Established conditions for your search.
 
Diagnosis CCMSweb Code
Galactosemia (aka: Classic Galactosemia; GALT Deficiency; Galactose-1-Phosphate Uridyl Transferase Deficiency) Galactosemia
Gaucher Disease Type III (Subacute/Chronic form, or "Atypical, due to Saposin C Deficiency") (aka: Gaucher Disease, Cardiovascular Form; Gaucher Disease, Type 3) Gaucher Disease Type III
Gaucher Disease, Type II ("Perinatal Lethal" or Colloidal Type) (aka: Gaucher Disease, Type 2; Glucocerebrosidase Deficiency; Glucosylceramidase Deficiency) Gaucher Disease, Type II
Generalized Anxiety Disorder (as defined within DC:0-3R, and diagnosed by specially-qualified professional as noted) [The person making the diagnosis must be a practicing medical or mental/behavioral health professional (i.e., physician, psychologist, psychiatrist, licensed clinical social worker, or DC:0-3R trained master's level clinician) who has taken at least the 1 1/2 to 2 day DC:0-3R Practitioner Preparation Course from a Colorado State recognized trainer; an overview or awareness level workshop does not make the person qualified.] Generalized Anxiety Disord
Glycinemia (aka: glycine encephalopathy; nonketotic hyperglycinemia; transient neonatal hyperglycinemia) Glycinemia
Gm1 Gangliosidosis (aka: Beta-Galactocidase-1 Deficiency; GLB1 Deficiency; Galactocidase, Beta-1; GLB1; Morquio Disease, Type B; Elastin-Binding Protein) Gm1Gangliosidosis
Griscelli Syndrome, type 1
 
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