40 Years of Experience
Accepting patients
Who is Dr. Abdenur, Clinical Biochemical Geneticist in Orange, CA?
Dr. Jose Abdenur, MD is a Clinical Biochemical Geneticist, who primarily practices in Orange, CA with 1 additional practice location. He has been practicing for over 40 years and is board certified by the American Board of Medical Genetics. Dr. Abdenur completed his residency at North Shore Univ Hosp, Pediatric Endocrinology. Dr. Abdenur is fluent in English and Spanish, and is currently seeing new patients. Dr. Abdenur’s practice accepts Kaiser Permanente, UnitedHealthcare, Aetna, Cigna and other major insurance plans. To book an appointment or to confirm insurance options, please call Dr. Abdenur’s office.
What are Areas of Expertise for Dr. Abdenur?
Dr. Jose Abdenur, MD is a highly-rated, board-certified Clinical Biochemical Geneticist known for expertly diagnosing, treating, and managing a wide array of related conditions or procedures. Utilizing the latest medical advancements and evidence-based practices, Dr. Abdenur empowers patients to confidently navigate their health journey, specializing in Inherited Metabolic Disorders, Metabolic Genetic Disorders, or comprehensive wellness support. Serving the Orange/CA community, Dr. Abdenur is dedicated to enhancing lives through expert, patient-centered care.
Where did Dr. Abdenur go to medical school and complete their residency?
Fellowship: Pedro Elizalde Children's Hospital | Biochemical Genetics: The Mount Sinai Hospital, Department of Pediatrics and Genetics, Mount Sinai School of Medicine, New York, NY, USA. The Children's Hospital and Biochemical Genetics Laboratory, Department of Pediatrics, University of Colorado Health | Human Genetics: The Mount Sinai Hospital Department of Pediatrics and Genetics, Mount Sinai School of Medicine, New York, NY, USA. | Pediatric Endocrinology, Metabolism and Nutrition: North Shore University Hospital, Department of Pediatrics, Cornell University Medical College, Manhasset, New York, USA
Residency: North Shore Univ Hosp, Pediatric Endocrinology | North Shore University Hospital | Pedro Elizalde Children's Hospital
Medical School: University De Buenos Aires- Fac De Med- Buenos Aires- Argentina | Universidad De Buenos Aires, Facultad De Ciencias Medicas
Is Dr. Abdenur board certified in Clinical Biochemical Geneticist?
Yes, Dr. Jose Abdenur, MD is board certified by the American Board of Medical Genetics
What languages does Dr. Abdenur speak?
Dr. Abdenur and their clinical team can communicate with patients in the following languages:
English
Spanish
What conditions does Dr. Abdenur treat?
As a Clinical Biochemical Geneticist, Dr. Abdenur 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. Abdenur. 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:
- Glycogen Storage Disease Type I
- Pompe Disease
- Glycogen Storage Disease
- Cori Disease
- Carbohydrate Metabolism Disorder
- Glycogen storage disease type I
- Pompe disease
- Glycogen storage disease type 0
- Glycogen storage disease type IV
- Glycogen storage disease type VI
- Glycogen storage disease type III
- von Gierke Disease
- GSD I
- Hepatorenal Glycogenosis
- GSD II
- Glycogen Storage Disease Type II
- Acid Maltase Deficiency
- GSD
- Glycogenosis
- Glycogen Storage Disease Type 0
- Glycogen Storage Disease Type IV
- GSD III
- Debrancher deficiency
ICD-10 Codes:
- E7401: von Gierke disease
- E7402: Pompe disease
- E7409: Other glycogen storage disease
- E7403: Cori disease
Also known as:
- Neuronal Ceroid Lipofuscinosis
- Genetic Brain Disorder
- CLN10 disease
- CLN11 disease
- CLN1 disease
- CLN2 disease
- CLN3 disease
- CLN4 disease
- CLN5 disease
- CLN6 disease
- CLN7 disease
- CLN8 disease
- NCL
- Batten disease
- Lysosomal Storage Disease
ICD-10 Codes:
- E754: Neuronal ceroid lipofuscinosis
Also known as:
- Mitochondrial Metabolism Disorder
- Mitochondrial Disease
- Mitochondrial neurogastrointestinal encephalopathy disease
- Neuropathy, ataxia, and retinitis pigmentosa
- Mitochondrial Metabolic Disease
- Energy Production Disorder
ICD-10 Codes:
- E8840: Mitochondrial metabolism disorder, unspecified
- E8849: Other mitochondrial metabolism disorders
Also known as:
- Propionic Acidemia
- Pyruvate Metabolism Disorder
- Metabolic Disorder
- Propionic acidemia
- Pyruvate carboxylase deficiency
- PA
- Propionyl-CoA Carboxylase Deficiency
- Gluconeogenesis disorder
- Pyruvate dehydrogenase deficiency
- Metabolism disorder
- Metabolic disease
- Body chemistry imbalance
ICD-10 Codes:
- E71121: Propionic acidemia
- E744: Disorders of pyruvate metabolism and gluconeogenesis
- E889: Metabolic disorder, unspecified
Also known as:
- Hurler Syndrome
- Hurler-Scheie Syndrome
- Carbohydrate Metabolism Disorder
- Mucopolysaccharidosis type I
- MPS IH
- Alpha-L-iduronidase deficiency
- Gargoylism
- MPS IH/S
- Intermediate MPS I
ICD-10 Codes:
- E7601: Hurler's syndrome
- E7602: Hurler-Scheie syndrome
Also known as:
- Mucopolysaccharidosis Type II
- Carbohydrate Metabolism Disorder
- Mucopolysaccharidosis type II
- MPS II
- Hunter syndrome
ICD-10 Codes:
- E761: Mucopolysaccharidosis, type II
Also known as:
- Nonketotic Hyperglycinemia
- Lysine and Hydroxylysine Metabolism Disorder
- Amino Acid Metabolism Disorder
- Nonketotic hyperglycinemia
- Hyperlysinemia
- NKH
- Glycine Encephalopathy
- Glycine Metabolism Disorder
- Lysine Processing Problems
- Genetic Lysine Disorder
ICD-10 Codes:
- E7251: Non-ketotic hyperglycinemia
- E723: Disorders of lysine and hydroxylysine metabolism
Also known as:
- Hereditary Ataxia
- Cerebellar Disorder
- Movement Disorder
- Genetic Ataxia
- Inherited Balance Disorder
- Familial Ataxia
ICD-10 Codes:
- G118: Other hereditary ataxias
Also known as:
- Genetic Risk for Other Disease
- Hereditary Disease Risk
- Increased Risk of Inherited Conditions
- Genetic Predisposition to Disease
ICD-10 Codes:
- Z1589: Genetic susceptibility to other disease
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
Also known as:
- X-linked Adrenoleukodystrophy
- Leukodystrophies
- X-linked adrenoleukodystrophy
- ALD
- Adrenoleukodystrophy
ICD-10 Codes:
- E71529: X-linked adrenoleukodystrophy, unspecified type
Also known as:
- Methylmalonic Acidemia
- Metabolic Disorder
- Methylmalonic acidemia
- MMA
- Methylmalonic Aciduria
- Methylmalonic Acidopathy
ICD-10 Codes:
- E71120: Methylmalonic acidemia
Which procedures does Dr. Abdenur perform as a Clinical Biochemical Geneticist?
As a Clinical Biochemical Geneticist, procedures performed by a Dr. Jose Abdenur may include:
- Biochemical Genetics Consultation
- Biochemical Genetics Follow Up
- Enzyme Replacement Therapy
- Genetic Testing
- Metabolic Assessment and Management
For detailed information, please contact Dr. Abdenur's office.
Does Dr. Abdenur accept my insurance?
Dr. Abdenur 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. Abdenur accept in Orange, CA?
Dr. Abdenur in Orange, CA accepts plans from many carriers. While this list is updated regularly, it is not a guarantee of coverage.
Top Insurances
All Other Third Party
Blue Shield of California
CalOptima
Centene
CVS Health (formerly Aetna)
Express Scripts
OptumRx
Other Health Care Provider
PIH Health
State of California
View All Insurances
Where is Dr. Abdenur's office located?
Recognitions
Awards
Agent of Change - Children and Families Commission of Orange County
What is Dr. Abdenur's NPI number?An National Provider Identifier (NPI) is a unique ID number that identifies doctors and healthcare providers nationwide.
Dr. Abdenur's National Provider Identifier (NPI) number is 1154428027.
What common questions do patients ask about Dr. Abdenur?
Here are answers to patients Frequently Asked Questions (FAQ’s) about Dr. Abdenur
What is Dr. Jose Abdenur's specialty?
Dr. Abdenur is a Clinical Biochemical Geneticist near Orange, CA. 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. Abdenur to book an appointment today.
Is this Dr. Jose Abdenur affiliated with a ranked Castle Connolly Top Hospital?
No, Abdenur is not affiliated with a Castle Connolly Top Hospital, but is affiliated with the following hospitals: Children’s Health of Orange County (CHOC). 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 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 Jose Abdenur accepting new patients in Orange, CA?
Yes, Dr. Jose Abdenur is accepting new patients at this time.
Does Dr. Jose Abdenur offer online booking?
Please contact Dr. Abdenur's office for information about online booking, telehealth, or to schedule an appointment.
How can I make an appointment with Jose Abdenur?
Please contact Dr. Abdenur's office for information regarding telehealth appointment availability or for scheduling assistance.
Which board certifications does Dr. Jose Abdenur have?
Dr. Jose Abdenur is certified by the American Board of Medical Genetics.
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