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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
Achondrogenesis I (Parenti-Fraccaro) Achondrogenesis I
Achondrogenesis II (Langer-Saldino) Achondrogenesis II
Acrocallosal Syndrome, Schinzel Type (aka: Schinzel Acrocallosal Syndrome; Acrocallosal Syndrome, Schinzel Type; ACLS; ACS; Hallux duplication, postaxial polydactyly, absence of the corpus callosum, severe mental retardation syndrome) Acrocallosal Synd, Schinzel
Acrodysostosis (aka: Arkless-Graham; Acrodysplasia; Maroteaux-Malamut; Peripheral Dysostosis-Nasal Hypoplasia-Mental Retardation Syndrome; PNM Syndrome) Acrodysostosis
Adrenoleukodystrophy (aka: ALD; AMN; X-ALD; Addison disease and cerebral sclerosis; Adrenomyeloneuropathy; Siemerling-creutzfeldt disease; Bronze schilder disease; Schilder Disease; Melanodermic Leukodystrophy; sudanophilic leukodystrophy; Pelizaeus Merzbacher Brain Sclerosis; Pelizaeus-Merzbacher Disease; PMD; Sclerosis, Diffuse Familial Brain; Sudanophilic Leukodystrophy, Pelizaeus-Merzbacher Type) Adrenoleukodystrophy
Agenesis of the Corpus Callosum (aka: Absence of the corpus callosum; Hypogenesis of the corpus callosum) Agenesis of Corpus Callosum
Aicardi Syndrome (aka: Agenesis of Corpus Callosum and Chorioretinal Abnormality; Agenesis of Corpus Callosum With Chorioretinitis Abnormality; Agenesis of Corpus Callosum With Infantile Spasms And Ocular Anomalies; Chorioretinal Anomalies with Agenesis of the Corpus Callosum; Callosal Agenesis and Ocular Abnormalities) Aicardi Synd
Alexander Disease Alexander Disease
Allan Herndon Syndrome (aka: Allan-Herndon-Dudley Syndrome (AHDS); Allan-Herndon-Dudley Mental Retardation) Allan Herndon Synd
Alper Disease (aka: Alper's Diffuse Degeneration of Cerebral Gray Matter with Hepatic Cirrhosis; Alpers Progressive Infantile Poliodystrophy; Christensen's disease; Christensen-Krabbe disease; Diffuse Cerebral Degeneration in Infancy; Poliodystrophia Cerebri Progressiva; Progressive Cerebral Poliodystrophy) Alper Disease
Amputation of the leg at the hip Amputation of leg at hip
Anencephaly Anencephaly
Angelman Syndrome (aka: AS) Angelman Synd
Aniridia Cerebellar Ataxia Mental Deficiency (aka: Gillespie syndrome; Aniridia, Partial-Cerebellar Ataxia-Oligophrenia; Aniridia-Cerebellar Ataxia-Mental Retardation)hrenia) Aniridia Cerebellar Ataxia MD
Anophthalmia, bilateral Anophthalmia, bilateral
Apert Syndrome (aka: ACS 1; ACS I; Acrocephalosyndactyly, Type I; Syndactylic Oxycephaly) Apert Synd
APGAR score of 3 or less at 20 minutes APGAR score 3 or less @ 20 min
Aphasia (with evidence of brain damage) (aka: aphemia with evidence of brain damage) Aphasia w brain damage
Argininosuccinic aciduria (aka: Arginino Succinase Deficiency; ASA Deficiency; Argininosuccinate Lyase Deficiency; ASL Deficiency) Argininosuccinic aciduria
Arthrogryposis (aka: arthrogryposis multiplex congenita; AMC; multiple congenital contractures) Arthrogryposis
Asphyxia (with evidence of brain damage within athe first couple days of the event) Asphyxia w brain damage
Ataxia Telangiectasia (aka: AT; Cerebello-Oculocutaneous Telangiectasia; Immunodeficiency with Ataxia Telangiectasia) Ataxia Telangiectasia
Autism Spectrum Disorder (aka: Infantile Autism; Kanner Syndrome; Autisitc Disorder; Asperger Syndrome; Asperger's Disorder; Pervasive Developmental Disorder; PDD; Pervasive Developmental Disorder-Not Otherwise Specified; PDD-NOS) Autism Spectrum Disorder
 
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