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Dr. Tomoyasu Higashimoto, DO, PHD

Ann Arbor, MI

Accepting patients

    Who is Dr. Higashimoto, Clinical Geneticist in Ann Arbor, MI?

    Dr. Tomoyasu Higashimoto, DO, PHD is a Clinical Geneticist, who primarily practices in Ann Arbor, MI with 2 additional practice locations. He is board certified. Dr. Higashimoto is fluent in English and Japanese, and is currently seeing new patients. Dr. Higashimoto’s practice accepts Medicaid, Medicare, UnitedHealthcare and other major insurance plans. To book an appointment or to confirm insurance options, please call Dr. Higashimoto’s office at (734) 240-8430.

    What languages does Dr. Higashimoto speak?

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

    • English

    • Japanese

    What conditions does Dr. Higashimoto treat?

    As a Clinical Geneticist, Dr. Higashimoto 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. Higashimoto. 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 for Family Planning
    • Genetic Counseling
    • Reproductive Genetic Counseling
    • Preconception Genetic Counseling
    • Family Planning Genetic Advice
    • Genetic risk assessment
    • Hereditary counseling
    • DNA counseling

    ICD-10 Codes:

    • Z315: Encounter for procreative genetic counseling
    • Z7183: Encounter for nonprocreative genetic counseling

    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:

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

    ICD-10 Codes:

    • F840: Autistic disorder

    Also known as:

    • Tyrosinemia
    • High Phenylalanine Levels
    • Metabolic Disorder
    • Tetrahydrobiopterin deficiency
    • Tyrosine Metabolism Disorder
    • Tyrosinosis
    • Hyperphenylalaninemia
    • Phenylalanine Metabolism Disorder
    • Phenylketonuria (PKU)

    ICD-10 Codes:

    • E7021: Tyrosinemia
    • E701: Other hyperphenylalaninemias

    Also known as:

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

    ICD-10 Codes:

    • Z713: Dietary counseling and surveillance

    Also known as:

    • Family History of Birth Defects or Genetic Disorder
    • Birth Defects
    • Family History
    • Genetic Disorder
    • Genetic risk for birth defects
    • Hereditary chromosomal abnormalities
    • Congenital anomalies in family

    ICD-10 Codes:

    • Z8279: Family history of other congenital malformations, deformations and chromosomal abnormalities

    Also known as:

    • Seizures
    • Epilepsy
    • Convulsions
    • Fits

    ICD-10 Codes:

    • R569: Unspecified convulsions

    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:

    • Failure to Thrive in Children
    • Growth Disorder
    • Poor growth in children
    • Childhood growth problems
    • Infant growth failure

    ICD-10 Codes:

    • R6251: Failure to thrive (child)

    Also known as:

    • Neurofibromatosis Type 1
    • Neurofibromatosis
    • Neurofibromatosis type 1
    • NF1
    • Von Recklinghausen disease
    • Peripheral neurofibromatosis

    ICD-10 Codes:

    • Q8501: Neurofibromatosis, type 1

    Also known as:

    • Family history of genetic disease carrier
    • Family History
    • Genetic Disorder
    • Inherited genetic disease risk
    • Genetic carrier status in family
    • Family history of inherited conditions

    ICD-10 Codes:

    • Z8481: Family history of carrier of genetic disease

    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:

    • 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:

    • Galactose Metabolism Disorder
    • Carbohydrate Metabolism Disorder
    • Galactosemia
    • Galactose Processing Problems
    • Genetic Galactose Disorder

    ICD-10 Codes:

    • E7429: Other disorders of galactose metabolism

    Also known as:

    • Family History of Epilepsy or Neurological Disease
    • Epilepsy
    • Family History
    • Neurologic Disease
    • Genetic risk for epilepsy
    • Hereditary nervous system disorders
    • Neurological conditions in family

    ICD-10 Codes:

    • Z820: Family history of epilepsy and other diseases of the nervous system

    Also known as:

    • Developmental Speech and Language Disorder
    • Speech and Communication Disorder
    • Childhood Language Delay
    • Global Speech Delay
    • Unspecified Communication Disorder

    ICD-10 Codes:

    • F809: Developmental disorder of speech and language, unspecified

    Also known as:

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

    ICD-10 Codes:

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

    Also known as:

    • Hereditary Hemorrhagic Telangiectasia
    • Bleeding Disorder
    • Hereditary hemorrhagic telangiectasia
    • Osler-Weber-Rendu Disease
    • HHT
    • Spider Veins

    ICD-10 Codes:

    • I780: Hereditary hemorrhagic telangiectasia

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

    As a Clinical Geneticist, procedures performed by a Dr. Tomoyasu Higashimoto may include:

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

    Does Dr. Higashimoto accept my insurance?

    Dr. Higashimoto accepts most major insurance plans. Important: Please call our office at (734) 240-8430 before your appointment to verify that your specific plan and network are accepted.

    What insurance plans does Dr. Higashimoto accept in Ann Arbor, MI?

    Dr. Higashimoto in Ann Arbor, MI accepts plans from many carriers. While this list is updated regularly, it is not a guarantee of coverage.

    Top Insurances

    • All Other Third Party

    • Blue Cross Blue Shield of Michigan

    • CVS Health (formerly Aetna)

    • Health Alliance Plan (HAP)

    • McLaren Health Plan

    • Medicaid

    • Medicare

    • Molina

    • Spectrum / Priority Health

    • UnitedHealthcare

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    Where is Dr. Higashimoto's office located?

    Dr. Tomoyasu Higashimoto's Primary Practice

    24 Frank Lloyd Wright Dr

    Ann Arbor, MI 48105

    (734) 240-8430

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    Dr. Tomoyasu Higashimoto's Practice 2

    1500 E Medical Center Dr Fl 3

    Ann Arbor, MI 48109

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    Dr. Tomoyasu Higashimoto's Practice 3

    1 William Carls Dr

    Commerce Township, MI 48382

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

    Dr. Higashimoto's National Provider Identifier (NPI) number is 1902219165.

    What common questions do patients ask about Dr. Higashimoto?

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

    What is Dr. Tomoyasu Higashimoto's specialty?

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

    Is this Dr. Tomoyasu Higashimoto affiliated with a ranked Castle Connolly Top Hospital?

    No, Higashimoto is not affiliated with a Castle Connolly Top Hospital, but is affiliated with the following hospitals: University Of Michigan Health - University Hospital. 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 Tomoyasu Higashimoto accepting new patients in Ann Arbor, MI?

    Yes, Dr. Tomoyasu Higashimoto is accepting new patients at this time.

    Does Dr. Tomoyasu Higashimoto offer online booking?

    Please contact Dr. Higashimoto's office at (734) 240-8430 for information about online booking, telehealth, or to schedule an appointment.

    How can I make an appointment with Tomoyasu Higashimoto?

    Please contact Dr. Higashimoto's office at (734) 240-8430 for information regarding telehealth appointment availability or for scheduling assistance.

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