MB
Accepting patients
Affiliated with a Castle Connolly Top Hospital
Who is Dr. Breilyn, Clinical Geneticist in New York, NY?
Dr. Margo Breilyn, MD is a Clinical Geneticist, who primarily practices in New York, NY with 2 additional practice locations. She is board certified. Dr. Breilyn is fluent in English and Spanish, and is currently seeing new patients. Dr. Breilyn’s practice accepts Medicare, UnitedHealthcare and other major insurance plans. To book an appointment or to confirm insurance options, please call Dr. Breilyn’s office at (212) 241-6947.
What languages does Dr. Breilyn speak?
Dr. Breilyn and their clinical team can communicate with patients in the following languages:
English
Spanish
What conditions does Dr. Breilyn treat?
As a Clinical Geneticist, Dr. Breilyn 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. Breilyn. 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
- Propionic Acidemia
- Maple Syrup Urine Disease
- Phenylketonuria (PKU)
- Branched-Chain Amino Acid Metabolism
- Tyrosinemia
- Urea Cycle Disorder
- Citrullinemia
- Argininemia
- Biotinidase Deficiency
- Pyruvate Metabolism Disorder
- Metabolic Disorder
- Tetrahydrobiopterin deficiency
- Propionic acidemia
- Maple syrup urine disease
- Phenylketonuria
- Arginase deficiency
- Immune System and Disorder
- Biotinidase deficiency
- Pyruvate carboxylase deficiency
- Hyperphenylalaninemia
- Phenylalanine Metabolism Disorder
- PA
- Propionyl-CoA Carboxylase Deficiency
- MSUD
- Branched-Chain Ketoaciduria
- PKU', 'Følling's Disease
- Phenylalanine Hydroxylase Deficiency
- Branched-Chain Amino Acid Disorders
- Branched-Chain Amino Acid Metabolism Condition
- Tyrosine Metabolism Disorder
- Tyrosinosis
- UCD
- Urea Cycle Enzyme Problem
- Ammonia Processing Disorder
- Argininosuccinic Aciduria
- Urea Cycle Disorder Type II
- Citrulline Disorder
- Arginase Deficiency
- Hyperargininemia
- BTD deficiency
- Biotin deficiency
- Genetic metabolic disorder
- Gluconeogenesis disorder
- Pyruvate dehydrogenase deficiency
ICD-10 Codes:
- E701: Other hyperphenylalaninemias
- E71121: Propionic acidemia
- E710: Maple-syrup-urine disease
- E700: Classical phenylketonuria
- E7119: Other disorders of branched-chain amino-acid metabolism
- E7021: Tyrosinemia
- E7220: Disorder of urea cycle metabolism, unspecified
- E7223: Citrullinemia
- E7221: Argininemia
- D81810: Biotinidase deficiency
- E744: Disorders of pyruvate metabolism and gluconeogenesis
Also known as:
- Glycogen Storage Disease Type I
- Glycogen Storage Disease
- Carbohydrate Metabolism Disorder
- Glycogen storage disease type I
- Glycogen storage disease type 0
- Glycogen storage disease type IV
- Glycogen storage disease type VI
- von Gierke Disease
- GSD I
- Hepatorenal Glycogenosis
- GSD
- Glycogenosis
- Glycogen Storage Disease Type 0
- Glycogen Storage Disease Type IV
ICD-10 Codes:
- E7401: von Gierke disease
- E7409: Other glycogen storage disease
Also known as:
- Ornithine Metabolism Disorder
- Homocystinuria
- Amino Acid Metabolism Disorder
- Ornithine translocase deficiency
- Ornithine Translocase Deficiency
- Hyperornithinemia
- Ornithine Processing Problems
- Cystathionine Beta-Synthase Deficiency
- CBS Deficiency
ICD-10 Codes:
- E724: Disorders of ornithine metabolism
- E7211: Homocystinuria
Also known as:
- Very Long-Chain Acyl-CoA Dehydrogenase Deficiency
- Medium-Chain Acyl-CoA Dehydrogenase Deficiency
- Lipid Metabolism Disorder
- Very long-chain acyl-CoA dehydrogenase deficiency
- Medium-chain acyl-CoA dehydrogenase deficiency
- VLCAD Deficiency
- Long-Chain Fatty Acid Oxidation Disorder
- VLCADD
- MCAD Deficiency
- Medium-Chain Fatty Acid Oxidation Disorder
- MCADD
ICD-10 Codes:
- E71310: Long chain/very long chain acyl CoA dehydrogenase deficiency
- E71311: Medium chain acyl CoA dehydrogenase deficiency
Also known as:
- Other Specific B Vitamin Deficiency
- B Vitamins
- Malnutrition
- Specific B Vitamin Shortage
- Less Common B Vitamin Deficiency
- Rare B Vitamin Deficiency
ICD-10 Codes:
- E538: Deficiency of other specified B group vitamins
Also known as:
- Carnitine Palmitoyltransferase II Deficiency
- Lipid Metabolism Disorder
- Carnitine palmitoyltransferase II deficiency
- CPT2 Deficiency
- Muscle CPT Deficiency
ICD-10 Codes:
- E71314: Muscle carnitine palmitoyltransferase deficiency
Also known as:
- Other Personal Health Risks
- Other health risk factors
- Specific personal risks
- Individual health concerns
ICD-10 Codes:
- Z9189: Other specified personal risk factors, not elsewhere classified
Which procedures does Dr. Breilyn perform as a Clinical Geneticist?
As a Clinical Geneticist, procedures performed by a Dr. Margo Breilyn may include:
- Biochemical Genetics Consultation
- Biochemical Genetics Follow Up
- Enzyme Replacement Therapy
- Genetic Testing
- Metabolic Assessment and Management
For detailed information, please contact Dr. Breilyn's office.
Does Dr. Breilyn accept my insurance?
Dr. Breilyn accepts most major insurance plans. Important: Please call our office at (212) 241-6947 before your appointment to verify that your specific plan and network are accepted.
What insurance plans does Dr. Breilyn accept in New York, NY?
Dr. Breilyn in New York, NY accepts plans from many carriers. While this list is updated regularly, it is not a guarantee of coverage.
Top Insurances
Centene
CVS Health (formerly Aetna)
Elevance Health Inc. (formerly Anthem)
EmblemHealth
Express Scripts
Healthfirst
Horizon BlueCross BlueShield
MetroPlus
State of New York
UnitedHealthcare
View All Insurances
Where is Dr. Breilyn's office located?
What is Dr. Breilyn's NPI number?An National Provider Identifier (NPI) is a unique ID number that identifies doctors and healthcare providers nationwide.
Dr. Breilyn's National Provider Identifier (NPI) number is 1932593464.
What common questions do patients ask about Dr. Breilyn?
Here are answers to patients Frequently Asked Questions (FAQ’s) about Dr. Breilyn
What is Dr. Margo Breilyn's specialty?
Dr. Breilyn is a Clinical Geneticist near New York, NY. A clinical geneticist is adept at offering thorough diagnostic, management, and counseling services for genetic disorders. Contact Dr. Breilyn to book an appointment today.
Is this Dr. Margo Breilyn affiliated with a ranked Castle Connolly Top Hospital?
Yes, Dr. Breilyn is affiliated with The Mount Sinai 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 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 Margo Breilyn accepting new patients in New York, NY?
Yes, Dr. Margo Breilyn is accepting new patients at this time.
Does Dr. Margo Breilyn offer online booking?
Please contact Dr. Breilyn's office at (212) 241-6947 for information about online booking, telehealth, or to schedule an appointment.
How can I make an appointment with Margo Breilyn?
Please contact Dr. Breilyn's office at (212) 241-6947 for information regarding telehealth appointment availability or for scheduling assistance.
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