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
Macrocephaly, Cutis Marmorata Telangiectatica Congenita Syndrome (aka: M-CMTC) Macrocephaly Cutis Marm T
Maple Syrup Urine Disease (where the diagnosis is late, or there is no or inadequate treatment) (aka: BCKD Deficiency, Branched Chain Alpha-Ketoacid Dehydrogenase Deficiency, Branched Chain Ketonuria I, Classical Maple Syrup Urine Disease) Maple Syrp Urine Dis,untreated
Marden Walker Syndrome Marden Walker Synd
Marinesco Sjogren Syndrome Marinesco Sjogren Synd
Marshall Smith Syndrome Marshall Smith Synd
Maxillofacial Dysostosis Maxillofacial Dysostosis
Meckel-Gruber Syndrome (aka: Meckel Syndrome (w/ skull defect); Dysencephalia Splanchnocystica) Meckel-Gruber Synd
Megalocornea Mental Retardation Syndrome (aka: MMR Syndrome; Neuhauser Syndrome) Megalocornea MR Synd
MELAS Syndrome MELAS Synd
Meningitis (including but not limited to the following types: Bacterial, Infantile, Neonatal, Meningococcal, Pneumococcal, Tuberculous, Epidemic Cerebrospinal, Pyogenic; Waterhouse-Friederichsen Syndrome) Meningitis
Menkes Syndrome (aka: Menkes Disease; Kinky Hair Disease) Menkes Synd
MERRF Syndrome MERRF Synd
MHBD Deficiency (a.k.a. 2-methyl-3-hydroxybutyryl-CoA Dehydrogenase Deficiency) MHBD Deficiency
Microcephaly Microcephaly
Moebius Sequence Moebius Sequence
Motor Neuron Disease Motor Neuron Disease
Mowat-Wilson Syndrome Mowat-Wilson Synd
Mucolipidosis IV Mucolipidosis IV
Mucopolysaccharidosis (except for type IVB) Mucopolysaccharidosis (not IVB)
Mucopolysaccharidosis VII (aka: Sly disease; Sly Syndrome; beta-glucuronidase deficiency) Mucopolysaccharidosis VII
Multiple Sulfatase Deficiency Multiple Sulfatase Deficiency
Multisystem Developmental Disorder (aka: MSDD) (as defined within DC:0-3R) [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.] Multisystem Dev Disord
Myasthenia Gravis (familial infantile type) Myasthenia Gravis
Myhre Syndrome Myhre Synd
Myoclonic Encephalopathy of Childhood (Kinsbourne Syndrome) Myoclonic Enceph of Childhood
Myopathy, Congenital Myopathy, Congenital
Myopathy, Congenital, Batten Turner Type Myopathy, Cong, Batten Turner
Myopathy, Desmin Storage (aka: DSM) Myopathy, Desmin Storage
Myopathy, Scapuloperoneal Myopathy, Scapuloperoneal
Myotonic dystrophy type 1 (aka: DM; DM1; Curschmann-Batten-Steinert syndrome; Steinert disease; dystrophia myotonia; myotonia atrophica) Myotonic dystrophy type 1
Myotubular Myopathy Myotubular Myopathy
 
  |  Website Feedback