ML
Accepting patients
Affiliated with a Castle Connolly Top Hospital
Who is Dr. Lopiccolo, Clinical Geneticist in New York, NY?
Dr. Mary Lopiccolo, MD is a Clinical Geneticist, who primarily practices in New York, NY. She is board certified. Dr. Lopiccolo is fluent in English, and is currently seeing new patients. Dr. Lopiccolo’s practice accepts Medicare, UnitedHealthcare and other major insurance plans. To book an appointment or to confirm insurance options, please call Dr. Lopiccolo’s office at (212) 241-6934.
What languages does Dr. Lopiccolo speak?
Dr. Lopiccolo and their clinical team can communicate with patients in the following languages:
English
What conditions does Dr. Lopiccolo treat?
As a Clinical Geneticist, Dr. Lopiccolo 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. Lopiccolo. 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
- Phenylketonuria (PKU)
- Maple Syrup Urine Disease
- Argininemia
- Propionic Acidemia
- Branched-Chain Amino Acid Metabolism
- Citrullinemia
- Biotinidase Deficiency
- Other Tyrosine Metabolism Disorder
- Metabolic Disorder
- Tetrahydrobiopterin deficiency
- Phenylketonuria
- Maple syrup urine disease
- Arginase deficiency
- Propionic acidemia
- Immune System and Disorder
- Biotinidase deficiency
- Alkaptonuria
- Hyperphenylalaninemia
- Phenylalanine Metabolism Disorder
- PKU', 'Følling's Disease
- Phenylalanine Hydroxylase Deficiency
- MSUD
- Branched-Chain Ketoaciduria
- Arginase Deficiency
- Hyperargininemia
- PA
- Propionyl-CoA Carboxylase Deficiency
- Branched-Chain Amino Acid Disorders
- Branched-Chain Amino Acid Metabolism Condition
- Argininosuccinic Aciduria
- Urea Cycle Disorder Type II
- Citrulline Disorder
- BTD deficiency
- Biotin deficiency
- Genetic metabolic disorder
- Tyrosine Processing Problems
ICD-10 Codes:
- E701: Other hyperphenylalaninemias
- E700: Classical phenylketonuria
- E710: Maple-syrup-urine disease
- E7221: Argininemia
- E71121: Propionic acidemia
- E7119: Other disorders of branched-chain amino-acid metabolism
- E7223: Citrullinemia
- D81810: Biotinidase deficiency
- E7029: Other disorders of tyrosine metabolism
Also known as:
- Ornithine Metabolism Disorder
- Lysine and Hydroxylysine Metabolism Disorder
- Amino Acid Metabolism Disorder
- Ornithine translocase deficiency
- Hyperlysinemia
- Ornithine Translocase Deficiency
- Hyperornithinemia
- Ornithine Processing Problems
- Lysine Processing Problems
- Genetic Lysine Disorder
ICD-10 Codes:
- E724: Disorders of ornithine metabolism
- E723: Disorders of lysine and hydroxylysine metabolism
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:
- Glutaric Acidemia Type II
- Carnitine Palmitoyltransferase II Deficiency
- Lipid Metabolism Disorder
- Glutaric acidemia type II
- Carnitine palmitoyltransferase II deficiency
- GA2
- Multiple Acyl-CoA Dehydrogenase Deficiency
- CPT2 Deficiency
- Muscle CPT Deficiency
ICD-10 Codes:
- E71313: Glutaric aciduria type II
- E71314: Muscle carnitine palmitoyltransferase 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:
- Rhabdomyolysis
- Muscle Disorder
- Muscle Breakdown
- Acute Muscle Injury
- Myoglobinuria
ICD-10 Codes:
- M6282: Rhabdomyolysis
Also known as:
- Autism
- Autism Spectrum Disorder
- Classic Autism', 'Kanner's Syndrome
- Severe Autism
ICD-10 Codes:
- F840: Autistic disorder
Also known as:
- Galactosemia
- Carbohydrate Metabolism Disorder
- Galactose intolerance
- Galactose metabolism disorder
- GALT deficiency
ICD-10 Codes:
- E7421: Galactosemia
Also known as:
- Carrier of Other Genetic Disease
- Genetic Disorder
- Hereditary Disease Carrier
- Rare Genetic Carrier
- Gene Carrier for Other Conditions
ICD-10 Codes:
- Z148: Genetic carrier of other disease
Also known as:
- Gaucher Disease
- Glucocerebrosidase deficiency', 'Gaucher's disease
- Genetic Metabolic Disorder
ICD-10 Codes:
- E7522: Gaucher disease
Which procedures does Dr. Lopiccolo perform as a Clinical Geneticist?
As a Clinical Geneticist, procedures performed by a Dr. Mary Lopiccolo may include:
- Biochemical Genetics Consultation
- Biochemical Genetics Follow Up
- Enzyme Replacement Therapy
- Genetic Testing
- Metabolic Assessment and Management
For detailed information, please contact Dr. Lopiccolo's office.
Does Dr. Lopiccolo accept my insurance?
Dr. Lopiccolo accepts most major insurance plans. Important: Please call our office at (212) 241-6934 before your appointment to verify that your specific plan and network are accepted.
What insurance plans does Dr. Lopiccolo accept in New York, NY?
Dr. Lopiccolo 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. Lopiccolo's office located?
What is Dr. Lopiccolo's NPI number?An National Provider Identifier (NPI) is a unique ID number that identifies doctors and healthcare providers nationwide.
Dr. Lopiccolo's National Provider Identifier (NPI) number is 1528565884.
What common questions do patients ask about Dr. Lopiccolo?
Here are answers to patients Frequently Asked Questions (FAQ’s) about Dr. Lopiccolo
What is Dr. Mary Lopiccolo's specialty?
Dr. Lopiccolo 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. Lopiccolo to book an appointment today.
Is this Dr. Mary Lopiccolo affiliated with a ranked Castle Connolly Top Hospital?
Yes, Dr. Lopiccolo 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 Mary Lopiccolo accepting new patients in New York, NY?
Yes, Dr. Mary Lopiccolo is accepting new patients at this time.
Does Dr. Mary Lopiccolo offer online booking?
Please contact Dr. Lopiccolo's office at (212) 241-6934 for information about online booking, telehealth, or to schedule an appointment.
How can I make an appointment with Mary Lopiccolo?
Please contact Dr. Lopiccolo's office at (212) 241-6934 for information regarding telehealth appointment availability or for scheduling assistance.
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