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Dr. Brandon Chalazan, MD, PHD

Chicago, IL

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    Who is Dr. Chalazan, Clinical Geneticist in Chicago, IL?

    Dr. Brandon Chalazan, MD, PHD is a Clinical Geneticist, who primarily practices in Chicago, IL. He is board certified. Dr. Chalazan is fluent in English, Polish, and Spanish, and is not currently seeing new patients. Dr. Chalazan’s practice accepts Medicare, UnitedHealthcare and other major insurance plans. To book an appointment or to confirm insurance options, please call Dr. Chalazan’s office at (604) 842-2306.

    What languages does Dr. Chalazan speak?

    Dr. Chalazan and their clinical team can communicate with patients in the following languages:

    • English

    • Polish

    • Spanish

    What conditions does Dr. Chalazan treat?

    As a Clinical Geneticist, Dr. Chalazan diagnoses, treats, and manages a wide range of conditions. This condition information is derived from anonymized insurance claims and highlights the medical conditions most commonly treated by Dr. Chalazan. It provides insight into the doctor’s areas of experience and expertise based on real-world patient encounters from the past two years, updated quarterly.

    Also known as:

    • Genetic Counseling
    • Genetic risk assessment
    • Hereditary counseling
    • DNA counseling

    ICD-10 Codes:

    • Z7183: Encounter for nonprocreative genetic counseling

    Also known as:

    • Propionic Acidemia
    • Maple Syrup Urine Disease
    • Other Metabolic Disorder
    • Isovaleric Acidemia
    • Metabolic Disorder
    • Propionic acidemia
    • Maple syrup urine disease
    • Isovaleric acidemia
    • PA
    • Propionyl-CoA Carboxylase Deficiency
    • MSUD
    • Branched-Chain Ketoaciduria
    • Uncommon Metabolic Condition
    • Rare Metabolic Disease
    • IVA
    • Isovaleric Aciduria

    ICD-10 Codes:

    • E71121: Propionic acidemia
    • E710: Maple-syrup-urine disease
    • E8889: Other specified metabolic disorders
    • E71110: Isovaleric acidemia

    Also known as:

    • Other Birth Defects Causing Short Stature
    • Other Genetic Syndrome
    • Birth Defects
    • Rare Short Stature Syndromes
    • Uncommon Dwarfism
    • Rare Birth Defect Syndromes
    • Uncommon Congenital Syndromes

    ICD-10 Codes:

    • Q8719: Other congenital malformation syndromes predominantly associated with short stature
    • Q8789: Other specified congenital malformation syndromes, not elsewhere classified

    Also known as:

    • Autism
    • Autism Spectrum Disorder
    • Classic Autism', 'Kanner's Syndrome
    • Severe Autism

    ICD-10 Codes:

    • F840: Autistic disorder

    Also known as:

    • Medium-Chain Acyl-CoA Dehydrogenase Deficiency
    • Very Long-Chain Acyl-CoA Dehydrogenase Deficiency
    • Lipid Metabolism Disorder
    • Medium-chain acyl-CoA dehydrogenase deficiency
    • Very long-chain acyl-CoA dehydrogenase deficiency
    • MCAD Deficiency
    • Medium-Chain Fatty Acid Oxidation Disorder
    • MCADD
    • VLCAD Deficiency
    • Long-Chain Fatty Acid Oxidation Disorder
    • VLCADD

    ICD-10 Codes:

    • E71311: Medium chain acyl CoA dehydrogenase deficiency
    • E71310: Long chain/very long chain acyl CoA dehydrogenase deficiency

    Also known as:

    • Child Development Problems
    • Child Development
    • Developmental concerns in children
    • Abnormal child development
    • Lack of normal development

    ICD-10 Codes:

    • R6250: Unspecified lack of expected normal physiological development in childhood

    Also known as:

    • Marfan Syndrome
    • MFS
    • Genetic connective tissue disorder
    • Fibrillinopathy

    ICD-10 Codes:

    • Q8740: Marfan syndrome, unspecified

    Also known as:

    • Ornithine Metabolism Disorder
    • Amino Acid Metabolism Disorder
    • Ornithine translocase deficiency
    • Ornithine Translocase Deficiency
    • Hyperornithinemia
    • Ornithine Processing Problems

    ICD-10 Codes:

    • E724: Disorders of ornithine metabolism

    Also known as:

    • Mitochondrial Metabolism Disorder
    • Mitochondrial Disease
    • Mitochondrial neurogastrointestinal encephalopathy disease
    • Neuropathy, ataxia, and retinitis pigmentosa
    • Mitochondrial Metabolic Disease
    • Energy Production Disorder

    ICD-10 Codes:

    • E8849: Other mitochondrial metabolism disorders

    Also known as:

    • Other Developmental Disabilities
    • Developmental Disabilities
    • Atypical psychological development
    • Unspecified developmental disorder

    ICD-10 Codes:

    • F88: Other disorders of psychological development

    Also known as:

    • Cori Disease
    • Carbohydrate Metabolism Disorder
    • Glycogen storage disease type III
    • GSD III
    • Debrancher deficiency

    ICD-10 Codes:

    • E7403: Cori disease

    Which procedures does Dr. Chalazan perform as a Clinical Geneticist?

    As a Clinical Geneticist, procedures performed by a Dr. Brandon Chalazan may include:

    For detailed information, please contact Dr. Chalazan's office.

    Does Dr. Chalazan accept my insurance?

    Dr. Chalazan accepts most major insurance plans. Important: Please call our office at (604) 842-2306 before your appointment to verify that your specific plan and network are accepted.

    What insurance plans does Dr. Chalazan accept in Chicago, IL?

    Dr. Chalazan in Chicago, IL accepts plans from many carriers. While this list is updated regularly, it is not a guarantee of coverage.

    Top Insurances

    • All Other Third Party

    • Centene

    • Cook County Health & Hospitals System

    • CVS Health (formerly Aetna)

    • Express Scripts

    • Health Care Service Corporation (HCSC)

    • Molina

    • Northshore University Healthsystem

    • State of Illinois

    • UnitedHealthcare

    View All Insurances

    Where is Dr. Chalazan's office located?

    Dr. Brandon Chalazan's Primary Practice

    225 E Chicago Ave

    Chicago, IL 60611

    (604) 842-2306

    Get Directions

    What is Dr. Chalazan's NPI number?An National Provider Identifier (NPI) is a unique ID number that identifies doctors and healthcare providers nationwide.

    Dr. Chalazan's National Provider Identifier (NPI) number is 1770364275.

    What common questions do patients ask about Dr. Chalazan?

    Here are answers to patients Frequently Asked Questions (FAQ’s) about Dr. Chalazan

    What is Dr. Brandon Chalazan's specialty?

    Dr. Chalazan is a Clinical Geneticist near Chicago, IL. A clinical geneticist is adept at offering thorough diagnostic, management, and counseling services for genetic disorders. Contact Dr. Chalazan to book an appointment today.

    Is this Dr. Brandon Chalazan affiliated with a ranked Castle Connolly Top Hospital?

    No, Chalazan is not affiliated with a Castle Connolly Top Hospital, but is affiliated with the following hospitals: Ann & Robert H. Lurie Childrens Hospital Of Chicago. Castle Connolly Top Hospitals are identified through a rigorous peer nomination process, evaluating factors like patient outcomes, quality of care, and expertise. The list recognizes hospitals that excel in 20 or more specific medical procedures, representing the top 25% nationwide. Castle Connolly Top Hospitals

    Where can I learn more about Clinical Geneticist?

    Explore Clinical Geneticist with insights from trusted medical experts on EverydayHealth.com, where you'll find the most relevant content and helpful condition guides for up-to date information about symptoms, causes, diagnosis, treatment and more. See all our health guides to find trusted information on medical conditions from our experts at Everyday Health.

    Is Brandon Chalazan accepting new patients in Chicago, IL?

    No, Dr. Brandon Chalazan is not accepting new patients at this time.

    Does Dr. Brandon Chalazan offer online booking?

    Please contact Dr. Chalazan's office at (604) 842-2306 for information about online booking, telehealth, or to schedule an appointment.

    How can I make an appointment with Brandon Chalazan?

    Please contact Dr. Chalazan's office at (604) 842-2306 for information regarding telehealth appointment availability or for scheduling assistance.

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