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Dr. Molly Mcpheron, MD

Indianapolis, IN

Accepting patients

Affiliated with a Castle Connolly Top Hospital

    Who is Dr. Mcpheron, Clinical Biochemical Geneticist in Indianapolis, IN?

    Dr. Molly Mcpheron, MD is a Clinical Biochemical Geneticist, who primarily practices in Indianapolis, IN with 2 additional practice locations. She is board certified. Dr. Mcpheron is fluent in English, and is currently seeing new patients. Dr. Mcpheron’s practice accepts Medicaid, Medicare, UnitedHealthcare and other major insurance plans. To book an appointment or to confirm insurance options, please call Dr. Mcpheron’s office at (317) 312-0119.

    What languages does Dr. Mcpheron speak?

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

    • English

    What conditions does Dr. Mcpheron treat?

    As a Clinical Biochemical Geneticist, Dr. Mcpheron 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. Mcpheron. 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:

    • High Phenylalanine Levels
    • Phenylketonuria (PKU)
    • Metabolic Disorder
    • Tetrahydrobiopterin deficiency
    • Phenylketonuria
    • Hyperphenylalaninemia
    • Phenylalanine Metabolism Disorder
    • PKU', 'Følling's Disease
    • Phenylalanine Hydroxylase Deficiency

    ICD-10 Codes:

    • E701: Other hyperphenylalaninemias
    • E700: Classical phenylketonuria

    Also known as:

    • Pompe Disease
    • Carbohydrate Metabolism Disorder
    • Pompe disease
    • GSD II
    • Glycogen Storage Disease Type II
    • Acid Maltase Deficiency

    ICD-10 Codes:

    • E7402: Pompe disease

    Also known as:

    • Fabry Disease
    • Genetic Brain Disorder
    • Fabry disease
    • Anderson-Fabry disease
    • Alpha-galactosidase A deficiency
    • Genetic Metabolic Disorder

    ICD-10 Codes:

    • E7521: Fabry (-Anderson) disease

    Also known as:

    • Other Long-Term Drug Therapy
    • Chronic medication use
    • Ongoing drug treatment
    • Extended drug therapy

    ICD-10 Codes:

    • Z79899: Other long term (current) drug therapy

    Also known as:

    • Mucopolysaccharidosis Type II
    • Carbohydrate Metabolism Disorder
    • Mucopolysaccharidosis type II
    • MPS II
    • Hunter syndrome

    ICD-10 Codes:

    • E761: Mucopolysaccharidosis, type II

    Also known as:

    • Nutrition Counseling
    • Nutrition
    • Dietary advice
    • Nutritional guidance
    • Healthy eating counseling

    ICD-10 Codes:

    • Z713: Dietary counseling and surveillance

    Also known as:

    • Mucopolysaccharidosis
    • Carbohydrate Metabolism Disorder
    • MPS
    • Lysosomal storage disease
    • GAG storage disease

    ICD-10 Codes:

    • E7629: Other mucopolysaccharidoses

    Also known as:

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

    ICD-10 Codes:

    • F840: Autistic disorder

    Also known as:

    • Other Abnormal Findings in Organ or Tissue Samples
    • Unusual Organ Test Results
    • Atypical Tissue Findings
    • Abnormal Specimen Analysis

    ICD-10 Codes:

    • R898: Other abnormal findings in specimens from other organs, systems and tissues

    Also known as:

    • Abnormal Newborn Screening Results
    • Newborn Screening
    • Positive newborn screen
    • Failed newborn screening
    • Newborn test abnormalities

    ICD-10 Codes:

    • P099: Abnormal findings on neonatal screening, 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:

    • Genetic Risk for Other Disease
    • Hereditary Disease Risk
    • Increased Risk of Inherited Conditions
    • Genetic Predisposition to Disease

    ICD-10 Codes:

    • Z1589: Genetic susceptibility to other disease

    Also known as:

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

    ICD-10 Codes:

    • E71311: Medium chain acyl CoA dehydrogenase deficiency

    Also known as:

    • Hurler-Scheie Syndrome
    • Carbohydrate Metabolism Disorder
    • Mucopolysaccharidosis type I
    • MPS IH/S
    • Alpha-L-iduronidase deficiency
    • Intermediate MPS I

    ICD-10 Codes:

    • E7602: Hurler-Scheie syndrome

    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:

    • Other Genetic Syndrome
    • Birth Defects
    • Rare Birth Defect Syndromes
    • Uncommon Congenital Syndromes

    ICD-10 Codes:

    • Q8789: Other specified congenital malformation syndromes, not elsewhere classified

    Also known as:

    • Immune Deficiency
    • Immune System and Disorder
    • Weak Immune System
    • Immune System Disorder

    ICD-10 Codes:

    • D849: Immunodeficiency, unspecified

    Also known as:

    • Newborn Respiratory Failure
    • Uncommon Infant and Newborn Problems
    • Neonatal Respiratory Failure
    • Infant Lung Failure
    • Newborn Breathing Crisis

    ICD-10 Codes:

    • P285: Respiratory failure of newborn

    Also known as:

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

    ICD-10 Codes:

    • F88: Other disorders of psychological development

    Which procedures does Dr. Mcpheron perform as a Clinical Biochemical Geneticist?

    As a Clinical Biochemical Geneticist, procedures performed by a Dr. Molly Mcpheron may include:

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

    Does Dr. Mcpheron accept my insurance?

    Dr. Mcpheron accepts most major insurance plans. Important: Please call our office at (317) 312-0119 before your appointment to verify that your specific plan and network are accepted.

    What insurance plans does Dr. Mcpheron accept in Indianapolis, IN?

    Dr. Mcpheron in Indianapolis, IN accepts plans from many carriers. While this list is updated regularly, it is not a guarantee of coverage.

    Top Insurances

    • All Other Third Party

    • Allied Benefit Systems

    • CareSource

    • Centene

    • Elevance Health Inc. (formerly Anthem)

    • Express Scripts

    • Medicaid

    • Medicare

    • State of Virginia

    • UnitedHealthcare

    View All Insurances

    Where is Dr. Mcpheron's office located?

    Dr. Molly Mcpheron's Primary Practice

    550 University Blvd

    Indianapolis, IN 46202

    (317) 312-0119

    Get Directions

    Dr. Molly Mcpheron's Practice 2

    575 Riley Hospital Dr

    Indianapolis, IN 46202

    (317) 944-3966

    Get Directions

    Dr. Molly Mcpheron's Practice 3

    702 Barnhill Dr

    Indianapolis, IN 46202

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

    Dr. Mcpheron's National Provider Identifier (NPI) number is 1225476930.

    What common questions do patients ask about Dr. Mcpheron?

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

    What is Dr. Molly Mcpheron's specialty?

    Dr. Mcpheron is a Clinical Biochemical Geneticist near Indianapolis, IN. A clinical biochemical geneticist is skilled in conducting and interpreting biochemical tests related to the diagnosis and management of genetic diseases. They serve as consultants on laboratory diagnoses for a wide variety of inherited disorders. Contact Dr. Mcpheron to book an appointment today.

    Is this Dr. Molly Mcpheron affiliated with a ranked Castle Connolly Top Hospital?

    Yes, Dr. Mcpheron is affiliated with Iu Health Methodist Hospital which is a Castle Connolly Top Hospital. Castle Connolly Top Hospitals are healthcare institutions recognized for their excellence in specific medical procedures and overall patient care. They 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 Biochemical Geneticist?

    Explore Clinical Biochemical 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 Molly Mcpheron accepting new patients in Indianapolis, IN?

    Yes, Dr. Molly Mcpheron is accepting new patients at this time.

    Does Dr. Molly Mcpheron offer online booking?

    Please contact Dr. Mcpheron's office at (317) 312-0119 for information about online booking, telehealth, or to schedule an appointment.

    How can I make an appointment with Molly Mcpheron?

    Please contact Dr. Mcpheron's office at (317) 312-0119 for information regarding telehealth appointment availability or for scheduling assistance.

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