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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
Dandy Walker Syndrome (aka: Dandy-Walker Cyst; Dandy-Walker Deformity; Hydrocephalus, Internal, Dandy-Walker Type; Hydrocephalus, Noncommunicating, Dandy-Walker Type; DWM; Luschka-Magendie Foramina Atresia) Dandy Walker Synd
De Barsy Syndrome (aka: Corneal Clouding-Cutis Laxa-Mental Retardation, Cutis Laxa-Growth Deficiency Syndrome; De Barsy-Moens-Diercks Syndrome; Progeroid Syndrome of De Barsy) De Barsy Synd
De Sanctis Cacchione Syndrome (aka: Xerodermic Idiocy) De Sanctis Cacchione Synd
Dejerine Sottas Disease (aka: Hereditary Motor Sensory Neuropathy Type III; HSMN Type III; Hypertrophic Interstitial Neuritis; Hypertrophic Interstitial Neuropathy; Hypertrophic Interstitial Radiculoneuropathy, Onion-Bulb Neuropathy) Dejerine Sottas Disease
Deletion 18p Syndrome (aka: Chromosome 18, Monosomy 18p; 18p Deletion Syndrome; 18p- Syndrome; Del(18p) Syndrome; Monosomy 18p Syndrome; Short Arm 18 Deletion Syndrome; Partial Deletion of Chromosome 18) Deletion 18p Synd
Deletion 18q syndrome (aka: Chromosome 18q- Syndrome; 18q Deletion Syndrome; 18q- Syndrome; Chromosome 18 Long Arm Deletion Syndrome; Chromosome 18, Monosomy 18Q; Del(18q) Syndrome; Monosomy 18q Syndrome; Partial Deletion of Chromosome 18) Deletion 18q Synd
Deletion 5p Syndrome (aka: Cri du chat Syndrome; Chromosome 5p-syndrome; Cat's Cry Syndrome; Chromosome 5, Monosomy 5p; Chromosome 5p-Syndrome; Le Jeune Syndrome; Partial Deletion of the Short Arm of Chromosome 5 Syndrome) Deletion 5p Synd
Deletion 9p Syndrome (aka: Chromosome 9, Partial Monosomy 9p; 9p Partial Monosomy; 9p- Syndrome, Partial; Chromosome 9, Partial Monosomy 9p22; Chromosome 9, Partial; Monosomy 9p22-pter; Del(9p) Syndrome, Partial; Deletion 9p Syndrome, Partial; Distal 9p- Syndrome; Distal Monosomy 9p; Monosomy 9p, Partial; Partial Deletion of Short Arm of Chromosome 9; 9p Deletion; 9p Minus Syndrome) Deletion 9p Synd
Depression of Infant and Early Childhood: Type I - Major Depression (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.] Depression: Type I-Major Dep
Deprivation/Maltreatment 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.] Deprivation/Maltreatment Dis
Diastrophic Dysplasia (aka: DD; DTD; Diastrophic Dwarfism; Diastrophic Nanism Syndrome) Diastrophic Dysplasia
Diencephalic Syndrome (aka: Diencephalic Syndrome of Childhood; Diencephalic Syndrome of Emaciation; Paramedian Diencephalic Syndrome; Russell's Diencephalic Cachexia; Russell's Syndrome) Diencephalic Synd
DOOR Syndrome (aka: DOOR(S) Syndrome; Deafness, Onychodystrophy, Osteodystrophy,and Mental Retardation) DOOR Synd
Down Syndrome (aka: Trisomy 21 Syndrome; Chromosome 21, Mosaic 21 Syndrome; Chromosome 21, Translocation 21 Syndrome; Trisomy G Syndrome) Down Synd
Dravet Syndrome (aka: severe myoclonic epilepsy of infancy; SMEI) Dravet Synd
Dubowitz Syndrome (aka: Intrauterine Dwarfism) Dubowitz Synd
Duchenne Muscular Dystrophy (aka: Childhood Muscular Dystrophy; DMD; Muscular Dystrophy (Classic X-linked Recessive); Progressive Muscular Dystrophy of Childhood; Pseudohypertrophic Muscular Dystrophy) Duchenne Muscular Dystrophy
Duplication 10q Syndrome (aka: Chromosome 10, distal trisomy 10q; Chromosome 10, Partial Trisomy 10q24-qter; Chromosome 10, Trisomy 10q2; Distal Duplication 10q; Distal Trisomy 10q Syndrome; Dup(10q) Syndrome) Duplication 10q Synd
Dyggve Melchior Clausen Syndrome (aka: DMC Disease; DMC Syndrome; Smith-McCort Dysplasia) Dyggve Melchior Clausen Synd
Dystonia Musculorum Deformans (aka: Torsion Dystonia) Dystonia Musculorum Deformans
 
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