Search
Public Awareness Materials Make A Referral
State-Approved Forms,
Instruction Manuals,
And Processes
Local Early Intervention Program Contacts

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.


A | B | C | D | E | F | G | H | I | J | K | L | M | N | O | P | Q | R | S | T | U | V | W | X | Y | Z
Search for:

Established conditions for your search.
 
Diagnosis CCMSweb Code
Fahr's Disease (aka: Cerebrovascular Ferrocalcinosis; Fahr Disease; Idiopathic Basal Ganglia Calcificationl; IBGC; Nonarteriosclerotic Cerebral Calcifications; SPD Calcinosis; Striopallidodentate Calcinosis) Fahr's Disease
Familial Mental Retardation Syndromes (incl: Familial Mental Retardation Syndrome ATR-16) Familial MR Synd
Farber Disease (aka: Farber's lipogranulomatosis; ceramidase deficiency) Farber Disease
Feeding Disorder Associated with Concurrent Medical Condition (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.] Feeding Disord w/ Med Cond
Feeding Disorder Associated with Insults to the Gastrointestinal Tract (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.] Feeding Disord w/ GI Tract
Feeding Disorder of Caregiver-Infant Reciprocity (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.] Feeding Disord of CG-Inf Rec
Feeding Disorder of State Regulation (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.] Feeding Disord of State Reg
Fetal Alcohol Syndrome (aka: FAS) Fetal Alcohol Synd
Fetal Hydantoin Syndrome (aka: Dilantin Embryopathy, Phenytoin Embryopathy) Fetal Hydantoin Synd
FG Syndrome (aka: Opitz-Kaveggia Syndrome) FG Synd
Fiber Type Disproportion, Congenital (aka: Atrophy of Type I Fibers; CFTD; CFTDM; Myopathy of Congenital Fiber Type Disproportion; Myopathy, Congenital, With Fiber-Type Disproportion) Fiber Type Disprop, Congenital
Fibrodysplasia Ossificans Progressiva (aka: FOP; Myositis Ossificans Progressiva) Fibrodysplasia Ossificans Prog
Filippi Syndrome (aka: Syndactyly Type I with Microcephaly and Mental Retardation ) Filippi Synd
Floating Harbor Syndrome (aka: FHS; Pelletier-Leisti syndrome) Floating Harbor Synd
Fountain Syndrome (aka: Mental Retardation-Deafness-Skeletal Abnormalities-Coarse Face with Full Lips) Fountain Synd
Fragile X Syndrome (aka: Fragile Site, Folic Acid Type, Rare; Fra(X)(Q27.3); Fragile X Mental Retardation Protein; FMRP; Fragile X Mental Retardation Syndrome; Marker X Syndrome; Martin-Bell Syndrome; Mental Retardation, X-Linked, Associated With Mar Xq28) Fragile X Synd
Friedreich's ataxia Friedreich's ataxia
Fryns Syndrome (aka: FRNS) Fryns Synd
Fucosidosis (aka: Alpha-L-Fucosidase Deficiency) Fucosidosis
Fukuyama Type Congenital Muscular Dystrophy (aka: Cerebromuscular Dystrophy, Fukuyama Type; Congenital Muscular Dystrophy, Fukuyama Type; FCMD; Micropolygyria With Muscular Dystrophy; Muscular Dystrophy, Congenital Progressive with Mental Retardation; Muscular Dystrophy, Congenital With Central Nervous System Involvement; Muscular Dystrophy, Congenital, Fukuyama Type; Muscular Dystrophy, Fukuyama Type) Fukuyama Type Cong Musc Dys
 
  |  Website Feedback