AK
Accepting patients
Affiliated with a Castle Connolly Top Hospital
Who is Dr. Kritzer, Clinical Geneticist in Boston, MA?
Dr. Amy Kritzer, MD is a Clinical Geneticist, who primarily practices in Boston, MA with 2 additional practice locations. She is board certified. Dr. Kritzer is fluent in English, and is currently seeing new patients. Dr. Kritzer’s practice accepts Cigna, Medicare, UnitedHealthcare and other major insurance plans. To book an appointment or to confirm insurance options, please call Dr. Kritzer’s office.
What languages does Dr. Kritzer speak?
Dr. Kritzer and their clinical team can communicate with patients in the following languages:
English
What conditions does Dr. Kritzer treat?
As a Clinical Geneticist, Dr. Kritzer 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. Kritzer. 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
- Citrullinemia
- Propionic Acidemia
- Biotinidase Deficiency
- Primary Carnitine Deficiency
- Phenylketonuria
- Metabolic Disorder
- Tetrahydrobiopterin deficiency
- Maple syrup urine disease
- Propionic acidemia
- Immune System and Disorder
- Biotinidase deficiency
- Primary carnitine deficiency
- PKU', 'Følling's Disease
- Phenylalanine Hydroxylase Deficiency
- Hyperphenylalaninemia
- Phenylalanine Metabolism Disorder
- MSUD
- Branched-Chain Ketoaciduria
- Argininosuccinic Aciduria
- Urea Cycle Disorder Type II
- Citrulline Disorder
- PA
- Propionyl-CoA Carboxylase Deficiency
- BTD deficiency
- Biotin deficiency
- Genetic metabolic disorder
- Systemic Primary Carnitine Deficiency
- Carnitine Uptake Defect
ICD-10 Codes:
- E700: Classical phenylketonuria
- E701: Other hyperphenylalaninemias
- E710: Maple-syrup-urine disease
- E7223: Citrullinemia
- E71121: Propionic acidemia
- D81810: Biotinidase deficiency
- E7141: Primary carnitine deficiency
Also known as:
- Medium-Chain Acyl-CoA Dehydrogenase Deficiency
- Very Long-Chain Acyl-CoA Dehydrogenase Deficiency
- Lipid Metabolism Disorder
- Medium-chain acyl-CoA dehydrogenase deficiency
- Very long-chain acyl-CoA dehydrogenase deficiency
- MCAD Deficiency
- Medium-Chain Fatty Acid Oxidation Disorder
- MCADD
- VLCAD Deficiency
- Long-Chain Fatty Acid Oxidation Disorder
- VLCADD
ICD-10 Codes:
- E71311: Medium chain acyl CoA dehydrogenase deficiency
- E71310: Long chain/very long chain acyl CoA dehydrogenase deficiency
Also known as:
- Autism
- Autism Spectrum Disorder
- Classic Autism', 'Kanner's Syndrome
- Severe Autism
ICD-10 Codes:
- F840: Autistic disorder
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:
- 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:
- 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:
- Smith-Lemli-Opitz Syndrome
- Glutaric Acidemia Type II
- Lipid Metabolism Disorder
- Smith-Lemli-Opitz syndrome
- Glutaric acidemia type II
- SLOS
- 7-dehydrocholesterol reductase deficiency
- Genetic Metabolic Disorder
- GA2
- Multiple Acyl-CoA Dehydrogenase Deficiency
ICD-10 Codes:
- E7872: Smith-Lemli-Opitz syndrome
- E71313: Glutaric aciduria type II
Also known as:
- Sanfilippo Syndrome
- Carbohydrate Metabolism Disorder
- Mucopolysaccharidosis type III
- MPS III
- Sanfilippo disease
ICD-10 Codes:
- E7622: Sanfilippo mucopolysaccharidoses
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:
- Mucopolysaccharidosis
- Carbohydrate Metabolism Disorder
- MPS
- Lysosomal storage disease
- GAG storage disease
ICD-10 Codes:
- E7629: Other mucopolysaccharidoses
Also known as:
- Methylmalonic Acidemia
- Metabolic Disorder
- Methylmalonic acidemia
- MMA
- Methylmalonic Aciduria
- Methylmalonic Acidopathy
ICD-10 Codes:
- E71120: Methylmalonic acidemia
Which procedures does Dr. Kritzer perform as a Clinical Geneticist?
As a Clinical Geneticist, procedures performed by a Dr. Amy Kritzer may include:
- Biochemical Genetics Consultation
- Biochemical Genetics Follow Up
- Enzyme Replacement Therapy
- Genetic Testing
- Metabolic Assessment and Management
For detailed information, please contact Dr. Kritzer's office.
Does Dr. Kritzer accept my insurance?
Dr. Kritzer 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. Kritzer accept in Boston, MA?
Dr. Kritzer in Boston, MA accepts plans from many carriers. While this list is updated regularly, it is not a guarantee of coverage.
Top Insurances
BCBS Unspecified
Blue Cross Blue Shield of Massachusetts
Boston Medical Center
Centene
CVS Health (formerly Aetna)
Independence Blue Cross
Point32Health
State of Massachusetts
State of Vermont
UnitedHealthcare
View All Insurances
Where is Dr. Kritzer's office located?
What is Dr. Kritzer's NPI number?An National Provider Identifier (NPI) is a unique ID number that identifies doctors and healthcare providers nationwide.
Dr. Kritzer's National Provider Identifier (NPI) number is 1700044336.
What common questions do patients ask about Dr. Kritzer?
Here are answers to patients Frequently Asked Questions (FAQ’s) about Dr. Kritzer
What is Dr. Amy Kritzer's specialty?
Dr. Kritzer 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. Kritzer to book an appointment today.
Is this Dr. Amy Kritzer affiliated with a ranked Castle Connolly Top Hospital?
Yes, Dr. Kritzer is affiliated with Dartmouth Hitchcock Medical Center, Dartmouth Hitchcock Medical Center which are a Castle Connolly Top Hospitals. 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 Amy Kritzer accepting new patients in Boston, MA?
Yes, Dr. Amy Kritzer is accepting new patients at this time.
Does Dr. Amy Kritzer offer online booking?
Please contact Dr. Kritzer's office for information about online booking, telehealth, or to schedule an appointment.
How can I make an appointment with Amy Kritzer?
Please contact Dr. Kritzer's office for information regarding telehealth appointment availability or for scheduling assistance.
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