JP
Accepting patients
Affiliated with a Castle Connolly Top Hospital
Who is Dr. Priestley, Clinical Biochemical Geneticist in Kentwood, MI?
Dr. Jessica Priestley, MD, PHD is a Clinical Biochemical Geneticist, who primarily practices in Kentwood, MI with 2 additional practice locations. She is board certified. Dr. Priestley is fluent in English, and is currently seeing new patients. Dr. Priestley’s practice accepts Medicare, UnitedHealthcare and other major insurance plans. To book an appointment or to confirm insurance options, please call Dr. Priestley’s office at (616) 391-2700.
What languages does Dr. Priestley speak?
Dr. Priestley and their clinical team can communicate with patients in the following languages:
English
What conditions does Dr. Priestley treat?
As a Clinical Biochemical Geneticist, Dr. Priestley 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. Priestley. 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
- Biotinidase Deficiency
- Phenylketonuria (PKU)
- Primary Carnitine Deficiency
- Metabolic Disorder
- Tetrahydrobiopterin deficiency
- Immune System and Disorder
- Biotinidase deficiency
- Phenylketonuria
- Primary carnitine deficiency
- Hyperphenylalaninemia
- Phenylalanine Metabolism Disorder
- BTD deficiency
- Biotin deficiency
- Genetic metabolic disorder
- PKU', 'Følling's Disease
- Phenylalanine Hydroxylase Deficiency
- Systemic Primary Carnitine Deficiency
- Carnitine Uptake Defect
ICD-10 Codes:
- E701: Other hyperphenylalaninemias
- D81810: Biotinidase deficiency
- E700: Classical phenylketonuria
- E7141: Primary carnitine deficiency
Also known as:
- Fabry Disease
- Genetic Brain Disorder
- Fabry disease
- Anderson-Fabry disease
- Alpha-galactosidase A deficiency
- Genetic Metabolic Disorder
ICD-10 Codes:
- E7521: Fabry (-Anderson) disease
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:
- Pompe Disease
- Carbohydrate Metabolism Disorder
- Pompe disease
- GSD II
- Glycogen Storage Disease Type II
- Acid Maltase Deficiency
ICD-10 Codes:
- E7402: Pompe disease
Also known as:
- Autism
- Autism Spectrum Disorder
- Classic Autism', 'Kanner's Syndrome
- Severe Autism
ICD-10 Codes:
- F840: Autistic disorder
Also known as:
- Special Medical Examination
- Specific health check
- Detailed medical assessment
- Special health screening
ICD-10 Codes:
- Z0189: Encounter for other specified special examinations
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:
- Other Genetic and Chromosomal Screening
- Genetic Testing
- Health Screening
- Additional Genetic Testing
- Advanced Chromosome Screening
- Specific Genetic Anomaly Screening
ICD-10 Codes:
- Z1379: Encounter for other screening for genetic and chromosomal anomalies
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:
- 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:
- 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:
- 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:
- Short Stature in Children
- Growth Disorder
- Child Growth Problems
- Dwarfism
- Growth Retardation
ICD-10 Codes:
- R6252: Short stature (child)
Also known as:
- Other Abnormal Findings in Organ or Tissue Samples
- Unusual Organ Test Results
- Atypical Tissue Findings
- Abnormal Specimen Analysis
ICD-10 Codes:
- R898: Other abnormal findings in specimens from other organs, systems and tissues
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:
- Chromosomal Abnormality
- Genetic Disorder
- Genetic Chromosome Disorder
- Chromosome Problem
- Aneuploidy
ICD-10 Codes:
- Q999: Chromosomal abnormality, unspecified
Which procedures does Dr. Priestley perform as a Clinical Biochemical Geneticist?
As a Clinical Biochemical Geneticist, procedures performed by a Dr. Jessica Priestley may include:
- Biochemical Genetics Consultation
- Biochemical Genetics Follow Up
- Enzyme Replacement Therapy
- Genetic Testing
- Metabolic Assessment and Management
For detailed information, please contact Dr. Priestley's office.
Does Dr. Priestley accept my insurance?
Dr. Priestley accepts most major insurance plans. Important: Please call our office at (616) 391-2700 before your appointment to verify that your specific plan and network are accepted.
What insurance plans does Dr. Priestley accept in Kentwood, MI?
Dr. Priestley in Kentwood, 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
ASR Corporation
Blue Cross Blue Shield of Michigan
CVS Health (formerly Aetna)
McLaren Health Plan
Medicare
Molina
Spectrum / Priority Health
State of Michigan
UnitedHealthcare
View All Insurances
Where is Dr. Priestley's office located?
Dr. Jessica Priestley's Primary Practice
4444 Kalamazoo Ave SE Ste 200
Kentwood, MI 49508
(616) 391-2700
Dr. Jessica Priestley's Practice 3
3401 Civic Center Blvd Rm 55
Philadelphia, PA 19104
(215) 590-1220
What is Dr. Priestley's NPI number?An National Provider Identifier (NPI) is a unique ID number that identifies doctors and healthcare providers nationwide.
Dr. Priestley's National Provider Identifier (NPI) number is 1366935439.
What common questions do patients ask about Dr. Priestley?
Here are answers to patients Frequently Asked Questions (FAQ’s) about Dr. Priestley
What is Dr. Jessica Priestley's specialty?
Dr. Priestley is a Clinical Biochemical Geneticist near Kentwood, MI. A clinical biochemical geneticist is skilled in conducting and interpreting biochemical tests related to the diagnosis and management of genetic diseases. They serve as consultants on laboratory diagnoses for a wide variety of inherited disorders. Contact Dr. Priestley to book an appointment today.
Is this Dr. Jessica Priestley affiliated with a ranked Castle Connolly Top Hospital?
Yes, Dr. Priestley is affiliated with Corewell Health Butterworth 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 Biochemical Geneticist?
Explore Clinical Biochemical 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 Jessica Priestley accepting new patients in Kentwood, MI?
Yes, Dr. Jessica Priestley is accepting new patients at this time.
Does Dr. Jessica Priestley offer online booking?
Please contact Dr. Priestley's office at (616) 391-2700 for information about online booking, telehealth, or to schedule an appointment.
How can I make an appointment with Jessica Priestley?
Please contact Dr. Priestley's office at (616) 391-2700 for information regarding telehealth appointment availability or for scheduling assistance.
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