EverydayHealthLogo
Dr. Robert Hopkin, MD

Dr. Robert Hopkin, MD

Toledo, OH

Accepting patients

    Who is Dr. Hopkin, Clinical Geneticist in Toledo, OH?

    Dr. Robert Hopkin, MD is a Clinical Geneticist, who primarily practices in Toledo, OH with 1 additional practice location. He is board certified by the American Board of Medical Genetics and American Board of Pediatrics. Dr. Hopkin graduated from University of Nevada, School of Medicine and completed his residency at Childrens Hosp Med Ctr, Medical Genetics; Phoenix Children'S Hosp, Pediatrics. Dr. Hopkin is fluent in English and French, and is currently seeing new patients. Dr. Hopkin’s practice accepts Medicare, UnitedHealthcare and other major insurance plans. To book an appointment or to confirm insurance options, please call Dr. Hopkin’s office.

    Where did Dr. Hopkin go to medical school and complete their residency?

    • Residency: Childrens Hosp Med Ctr, Medical Genetics; Phoenix Children'S Hosp, Pediatrics | Phoenix Children's Hospital Program

    • Medical School: University of Nv Sch of Med, Reno Nv | University of Nevada, School of Medicine

    Is Dr. Hopkin board certified in Clinical Geneticist?

    Yes, Dr. Robert Hopkin, MD is board certified by the American Board of Medical Genetics , American Board of Pediatrics

    What languages does Dr. Hopkin speak?

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

    • English

    • French

    What conditions does Dr. Hopkin treat?

    As a Clinical Geneticist, Dr. Hopkin 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. Hopkin. 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:

    • Fabry Disease
    • Gaucher Disease
    • Genetic Brain Disorder
    • Fabry disease
    • Anderson-Fabry disease
    • Alpha-galactosidase A deficiency
    • Genetic Metabolic Disorder
    • Glucocerebrosidase deficiency', 'Gaucher's disease

    ICD-10 Codes:

    • E7521: Fabry (-Anderson) disease
    • E7522: Gaucher disease

    Also known as:

    • 22q11.2 Deletion Syndrome
    • Autosomal Deletion Syndrome
    • Extra Chromosome
    • Other Chromosomal Abnormality
    • Genetic Disorder
    • 22q11.2 deletion syndrome
    • Velo-Cardio-Facial Syndrome
    • DiGeorge Syndrome
    • Catch 22 Syndrome
    • Autosomal Microdeletion
    • Chromosome Deletion
    • Genetic Deletion
    • Trisomy
    • Partial Trisomy
    • Autosomal Trisomy
    • Rare Chromosome Disorder
    • Atypical Chromosomal Condition
    • Genetic Chromosome Problem

    ICD-10 Codes:

    • Q9381: Velo-cardio-facial syndrome
    • Q9389: Other deletions from the autosomes
    • Q928: Other specified trisomies and partial trisomies of autosomes
    • Q998: Other specified chromosome abnormalities

    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:

    • 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:

    • 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:

    • Mucopolysaccharidosis Type II
    • Sanfilippo Syndrome
    • Carbohydrate Metabolism Disorder
    • Mucopolysaccharidosis type II
    • Mucopolysaccharidosis type III
    • MPS II
    • Hunter syndrome
    • MPS III
    • Sanfilippo disease

    ICD-10 Codes:

    • E761: Mucopolysaccharidosis, type II
    • E7622: Sanfilippo mucopolysaccharidoses

    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:

    • Glycoprotein Degradation Disorder
    • Carbohydrate Metabolism Disorder
    • Aspartylglucosaminuria
    • Fucosidosis
    • Genetic metabolic disorder

    ICD-10 Codes:

    • E771: Defects in glycoprotein degradation

    Also known as:

    • Hurler Syndrome
    • Carbohydrate Metabolism Disorder
    • Mucopolysaccharidosis type I
    • MPS IH
    • Alpha-L-iduronidase deficiency
    • Gargoylism

    ICD-10 Codes:

    • E7601: Hurler's syndrome

    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:

    • Intellectual Disability
    • Developmental Disabilities
    • Cognitive Impairment
    • Developmental Delay
    • Learning Disability (General)

    ICD-10 Codes:

    • F79: Unspecified intellectual disabilities

    Also known as:

    • Morquio A Syndrome
    • Carbohydrate Metabolism Disorder
    • Mucopolysaccharidosis type IV
    • MPS IVA
    • Morquio syndrome type A
    • N-acetylgalactosamine-6-sulfatase deficiency

    ICD-10 Codes:

    • E76210: Morquio A mucopolysaccharidoses

    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:

    • Lipid Storage Disorder
    • Metabolic Disorder
    • Cerebrotendinous xanthomatosis
    • Lipidosis
    • Fat storage disease

    ICD-10 Codes:

    • E755: Other lipid storage disorders

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

    As a Clinical Geneticist, procedures performed by a Dr. Robert Hopkin may include:

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

    Does Dr. Hopkin accept my insurance?

    Dr. Hopkin accepts most major insurance plans. Important: Please call our office at before your appointment to verify that your specific plan and network are accepted.

    What insurance plans does Dr. Hopkin accept in Toledo, OH?

    Dr. Hopkin in Toledo, OH accepts plans from many carriers. While this list is updated regularly, it is not a guarantee of coverage.

    Top Insurances

    • All Other Third Party

    • CareSource

    • Centene

    • CVS Health (formerly Aetna)

    • Elevance Health Inc. (formerly Anthem)

    • Medicare

    • Molina

    • State of Indiana

    • State of Ohio

    • UnitedHealthcare

    View All Insurances

    Where is Dr. Hopkin's office located?

    Dr. Robert Hopkin's Primary Practice

    2150 W Central Ave

    Toledo, OH 43606

    Get Directions

    Dr. Robert Hopkin's Practice 2

    3333 Burnet Ave

    Cincinnati, OH 45229

    Get Directions

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

    Dr. Hopkin's National Provider Identifier (NPI) number is 1447281878.

    What common questions do patients ask about Dr. Hopkin?

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

    What is Dr. Robert Hopkin's specialty?

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

    Is this Dr. Robert Hopkin affiliated with a ranked Castle Connolly Top Hospital?

    No, Hopkin is not affiliated with a Castle Connolly Top Hospital, but is affiliated with the following hospitals: Cincinnati Childrens - Burnet Campus. 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 Robert Hopkin accepting new patients in Toledo, OH?

    Yes, Dr. Robert Hopkin is accepting new patients at this time.

    Does Dr. Robert Hopkin offer online booking?

    Please contact Dr. Hopkin's office for information about online booking, telehealth, or to schedule an appointment.

    How can I make an appointment with Robert Hopkin?

    Please contact Dr. Hopkin's office for information regarding telehealth appointment availability or for scheduling assistance.

    Which board certifications does Dr. Robert Hopkin have?

    Dr. Robert Hopkin is certified by the American Board of Medical Genetics and American Board of Pediatrics.

    Other Clinical Geneticist Near Toledo, OH

    JP

    Clinical Geneticist

    acceptingPatients-iconAccepting patients
    Toledo, OH
    MM

    Clinical Cytogeneticist

    acceptingPatients-iconAccepting patients
    Toledo, OH
    Dr. Nastaran Foyouzi-Yousefi, MD

    Reproductive Endocrinologist

    acceptingPatients-iconAccepting patients
    telehealth-iconTelehealth
    Ann Arbor, MI
    See All Specialists

    Doctors by Category

    Specialists