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Dr. Catherine Keegan, MD, PHD

Ann Arbor, MI

Accepting patients

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

    Dr. Catherine Keegan, MD, PHD is a Clinical Geneticist, who primarily practices in Ann Arbor, MI with 1 additional practice location. She is board certified by the American Board of Medical Genetics and American Board of Pediatrics. Dr. Keegan completed her residency at Univ Of Mi Hosps & Hlth Ctrs, Medical Genetics; Children'S Hosp, Pediatrics. Dr. Keegan is fluent in English, and is currently seeing new patients. Dr. Keegan’s practice accepts Medicaid, Medicare, UnitedHealthcare and other major insurance plans. To book an appointment or to confirm insurance options, please call Dr. Keegan’s office at (586) 979-1060.

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

    • Residency: Univ Of Mi Hosps & Hlth Ctrs, Medical Genetics; Children'S Hosp, Pediatrics

    • Medical School: University of Mi Med Sch

    Is Dr. Keegan board certified in Clinical Geneticist?

    Yes, Dr. Catherine Keegan, MD, PHD is board certified by the American Board of Medical Genetics , American Board of Pediatrics

    What languages does Dr. Keegan speak?

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

    • English

    What conditions does Dr. Keegan treat?

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

    • 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:

    • Other Developmental Disabilities
    • Developmental Coordination Disorder
    • Developmental Disabilities
    • Atypical psychological development
    • Unspecified developmental disorder
    • Dyspraxia
    • Motor Skill Disorder
    • Clumsiness Syndrome

    ICD-10 Codes:

    • F88: Other disorders of psychological development
    • F82: Specific developmental disorder of motor function

    Also known as:

    • Failure to Thrive in Children
    • Short Stature in Children
    • Growth Disorder
    • Poor growth in children
    • Childhood growth problems
    • Infant growth failure
    • Child Growth Problems
    • Dwarfism
    • Growth Retardation

    ICD-10 Codes:

    • R6251: Failure to thrive (child)
    • R6252: Short stature (child)

    Also known as:

    • Multiple Birth Defects
    • Other Genetic Syndrome
    • Birth Defects
    • Complex congenital anomalies
    • Multiple congenital anomalies
    • Syndromic birth defects
    • Rare Birth Defect Syndromes
    • Uncommon Congenital Syndromes

    ICD-10 Codes:

    • Q897: Multiple congenital malformations, not elsewhere classified
    • Q8789: Other specified congenital malformation syndromes, not elsewhere classified

    Also known as:

    • Family History of Breast Cancer
    • Breast Cancer
    • Family History
    • Hereditary breast cancer risk
    • Genetic predisposition to breast cancer
    • Breast cancer in the family

    ICD-10 Codes:

    • Z803: Family history of malignant neoplasm of breast

    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:

    • 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:

    • 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:

    • Cafe-au-lait Spots
    • Birthmarks
    • CALMs
    • Coffee-with-Milk Spots
    • Light Brown Birthmarks

    ICD-10 Codes:

    • L813: Cafe au lait spots

    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:

    • 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:

    • Other Muscle Disorder
    • Muscle Disorder
    • Various Muscle Conditions
    • Uncommon Muscle Problems
    • Specific Muscle Ailments

    ICD-10 Codes:

    • M6289: Other specified disorders of muscle

    Also known as:

    • ADHD, Combined Type
    • Attention Deficit Hyperactivity Disorder
    • Attention-deficit/hyperactivity disorder
    • Combined ADHD
    • Typical ADHD

    ICD-10 Codes:

    • F902: Attention-deficit hyperactivity disorder, combined type

    Also known as:

    • Turner Syndrome
    • Monosomy X
    • 45,X Karyotype
    • Ullrich-Turner Syndrome

    ICD-10 Codes:

    • Q969: Turner's syndrome, unspecified

    Also known as:

    • Macrocephaly
    • Craniofacial Abnormality
    • Large head size
    • Enlarged head
    • Big head syndrome

    ICD-10 Codes:

    • Q753: Macrocephaly

    Also known as:

    • Other General Family Planning Counseling
    • Additional Reproductive Health Advice
    • Comprehensive Procreation Guidance
    • Advanced Fertility Planning Counseling

    ICD-10 Codes:

    • Z3169: Encounter for other general counseling and advice on procreation

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

    As a Clinical Geneticist, procedures performed by a Dr. Catherine Keegan may include:

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

    Does Dr. Keegan accept my insurance?

    Dr. Keegan accepts most major insurance plans. Important: Please call our office at (586) 979-1060 before your appointment to verify that your specific plan and network are accepted.

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

    Dr. Keegan 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)

    • Express Scripts

    • McLaren Health Plan

    • Medicaid

    • Molina

    • Spectrum / Priority Health

    • UnitedHealthcare

    • Upper Peninsula Health Plan

    View All Insurances

    Where is Dr. Keegan's office located?

    Dr. Catherine Keegan's Primary Practice

    1500 E Medical Center Dr Fl 6

    Ann Arbor, MI 48109

    (586) 979-1060

    Get Directions

    Dr. Catherine Keegan's Practice 2

    1200 E Michigan Ave Ste 460

    Lansing, MI 48912

    Get Directions

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

    Dr. Keegan's National Provider Identifier (NPI) number is 1144230764.

    What common questions do patients ask about Dr. Keegan?

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

    What is Dr. Catherine Keegan's specialty?

    Dr. Keegan 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. Keegan to book an appointment today.

    Is this Dr. Catherine Keegan affiliated with a ranked Castle Connolly Top Hospital?

    No, Keegan 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 Catherine Keegan accepting new patients in Ann Arbor, MI?

    Yes, Dr. Catherine Keegan is accepting new patients at this time.

    Does Dr. Catherine Keegan offer online booking?

    Please contact Dr. Keegan's office at (586) 979-1060 for information about online booking, telehealth, or to schedule an appointment.

    How can I make an appointment with Catherine Keegan?

    Please contact Dr. Keegan's office at (586) 979-1060 for information regarding telehealth appointment availability or for scheduling assistance.

    Which board certifications does Dr. Catherine Keegan have?

    Dr. Catherine Keegan is certified by the American Board of Medical Genetics and American Board of Pediatrics.

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