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Dr. Stephanie Sacharow, MD

Dr. Stephanie Sacharow, MD

Boston, MA

17 Years of Experience

Accepting patients

    Who is Dr. Sacharow, Clinical Geneticist in Boston, MA?

    Dr. Stephanie Sacharow, MD is a Clinical Geneticist, who primarily practices in Boston, MA. She has been practicing for over 17 years and is board certified by the American Board of Medical Genetics and American Board of Pediatrics. Dr. Sacharow completed her residency at University of Miami Affiliated Hospitals. Dr. Sacharow is fluent in English, and is currently seeing new patients. Dr. Sacharow’s practice accepts Medicaid, Medicare, UnitedHealthcare and other major insurance plans. To book an appointment or to confirm insurance options, please call Dr. Sacharow’s office at (617) 355-6000.

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

    • Fellowship: MEDICAL GENETICS, UNIVERSITY OF MIAMI, MIAMI, FL

    • Residency: University of Miami Affiliated Hospitals

    Is Dr. Sacharow board certified in Clinical Geneticist?

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

    What languages does Dr. Sacharow speak?

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

    • English

    What conditions does Dr. Sacharow treat?

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

    • Phenylketonuria (PKU)
    • High Phenylalanine Levels
    • Maple Syrup Urine Disease
    • Phenylketonuria
    • Metabolic Disorder
    • Tetrahydrobiopterin deficiency
    • Maple syrup urine disease
    • PKU', 'Følling's Disease
    • Phenylalanine Hydroxylase Deficiency
    • Hyperphenylalaninemia
    • Phenylalanine Metabolism Disorder
    • MSUD
    • Branched-Chain Ketoaciduria

    ICD-10 Codes:

    • E700: Classical phenylketonuria
    • E701: Other hyperphenylalaninemias
    • E710: Maple-syrup-urine disease

    Also known as:

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

    ICD-10 Codes:

    • F840: Autistic disorder

    Also known as:

    • Delayed Child Development
    • Child Development Problems
    • Child Development
    • Developmental delay
    • Slow development in children
    • Milestone delays
    • Developmental concerns in children
    • Abnormal child development
    • Lack of normal development

    ICD-10 Codes:

    • R620: Delayed milestone in childhood
    • R6250: Unspecified lack of expected normal physiological development in childhood

    Also known as:

    • Extra Chromosome
    • Chromosomal Abnormality
    • Genetic Disorder
    • Trisomy
    • Partial Trisomy
    • Autosomal Trisomy
    • Genetic Chromosome Disorder
    • Chromosome Problem
    • Aneuploidy

    ICD-10 Codes:

    • Q928: Other specified trisomies and partial trisomies of autosomes
    • Q999: Chromosomal abnormality, unspecified

    Also known as:

    • Short Stature in Children
    • Growth Disorder
    • Child Growth Problems
    • Dwarfism
    • Growth Retardation

    ICD-10 Codes:

    • R6252: Short stature (child)

    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:

    • Unspecified Abnormal Finding in Organs or Tissues
    • General abnormal tissue test
    • Unspecified organ abnormality
    • Abnormal body system finding

    ICD-10 Codes:

    • R899: Unspecified abnormal finding in specimens from other organs, systems and tissues

    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:

    • Face and Neck Birth Defect
    • Craniofacial Abnormality
    • Neck Injuries and Disorder
    • Congenital Facial Anomaly
    • Neck Malformation at Birth
    • Craniofacial Birth Defect

    ICD-10 Codes:

    • Q189: Congenital malformation of face and neck, unspecified

    Also known as:

    • Hereditary Alpha Tryptasemia
    • High Tryptase Levels
    • Genetic Tryptase Disorder
    • Familial Tryptasemia

    ICD-10 Codes:

    • D8944: Hereditary alpha tryptasemia

    Also known as:

    • Joint Hypermobility Syndrome
    • Connective Tissue Disorder
    • Benign Joint Hypermobility Syndrome
    • Double-Jointedness
    • Hypermobility Spectrum Disorder

    ICD-10 Codes:

    • M357: Hypermobility syndrome

    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:

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

    ICD-10 Codes:

    • Q753: Macrocephaly

    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:

    • 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:

    • 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

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

    As a Clinical Geneticist, procedures performed by a Dr. Stephanie Sacharow may include:

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

    Does Dr. Sacharow accept my insurance?

    Dr. Sacharow accepts most major insurance plans. Important: Please call our office at (617) 355-6000 before your appointment to verify that your specific plan and network are accepted.

    What insurance plans does Dr. Sacharow accept in Boston, MA?

    Dr. Sacharow in Boston, MA accepts plans from many carriers. While this list is updated regularly, it is not a guarantee of coverage.

    Top Insurances

    • Blue Cross Blue Shield of Massachusetts

    • Boston Medical Center

    • CVS Health (formerly Aetna)

    • Fallon Community Health Plan

    • Health Plans

    • Independence Blue Cross

    • Medicare

    • Point32Health

    • State of Massachusetts

    • UnitedHealthcare

    View All Insurances

    Where is Dr. Sacharow's office located?

    Dr. Stephanie Sacharow's Primary Practice

    300 Longwood Ave

    Boston, MA 02115

    (617) 355-6000

    Get Directions

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

    Dr. Sacharow's National Provider Identifier (NPI) number is 1134328982.

    What common questions do patients ask about Dr. Sacharow?

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

    What is Dr. Stephanie Sacharow's specialty?

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

    Is this Dr. Stephanie Sacharow affiliated with a ranked Castle Connolly Top Hospital?

    No, Sacharow is not affiliated with a Castle Connolly Top Hospital, but is affiliated with the following hospitals: Boston Childrens 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 Stephanie Sacharow accepting new patients in Boston, MA?

    Yes, Dr. Stephanie Sacharow is accepting new patients at this time.

    Does Dr. Stephanie Sacharow offer online booking?

    Please contact Dr. Sacharow's office at (617) 355-6000 for information about online booking, telehealth, or to schedule an appointment.

    How can I make an appointment with Stephanie Sacharow?

    Please contact Dr. Sacharow's office at (617) 355-6000 for information regarding telehealth appointment availability or for scheduling assistance.

    Which board certifications does Dr. Stephanie Sacharow have?

    Dr. Stephanie Sacharow is certified by the American Board of Medical Genetics and American Board of Pediatrics.

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