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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
Hallervorden-Spatz Disease (aka: Pantothenate kinase-associated neurodegeneration; PKAN) Hallervorden-Spatz Disease
Hallgren Syndrome Hallgren Synd
Hearing Loss (diagnosis with bilateral hearing loss) Hearing Loss (bilateral loss)
Hemimegalencephaly Hemimegalencephaly
HIV (where the child's status of the HIV infecton has been confirmed) HIV (confirmed)
Holoporencephaly (aka: Alobar Holoprosencephaly; Arhinencephaly; Familial Alobar Holoprosencephaly; HS; Holoprosencephaly Malformation Complex; Holoprosencephaly Sequence; Lobar Holoprosencephaly; Semilobar Holoprosencephaly) Holoporencephaly
Homocystinuria Homocystinuria
Human HOXA1 Syndromes (aka: Athabaskan Brainstem Dysgenesis Syndrome (ABDS); Navajo Brainstem Syndrome; Bosley-Salih-Alorainy Syndrome; BSAS) Human HOXA1 Synds
Hunter Syndrome (aka: MPSII, MPS Disorder II, Mucopolysaccharidosis Type II) Hunter Synd
Hurler Syndrome (aka: Mucopolysaccharidosis Type I; MPS I-H; MPS1) Hurler Synd
Hydranencephaly Hydranencephaly
Hydrocephalus, Congenital (aka: Benign Hydrocephalus, Communicating Hydrocephalus, Internal Hydrocephalus, Non-Communicating Hydrocephalus, Normal Pressure Hydrocephalus, Obstructive Hydrocephalus) Hydrocephalus, Congenital
Hypomelanosis of Ito (aka: Incontinentia pigmentosa acromians) Hypomelanosis of Ito
 
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