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Accepting patients
Who is Dr. Baker, Clinical Geneticist in Omaha, NE?
Dr. Craig Baker, MD is a Clinical Geneticist, who primarily practices in Omaha, NE with 2 additional practice locations. He is board certified. Dr. Baker is fluent in English and Spanish, and is currently seeing new patients. Dr. Baker’s practice accepts Medicare, UnitedHealthcare and other major insurance plans. To book an appointment or to confirm insurance options, please call Dr. Baker’s office at (402) 559-6403.
What languages does Dr. Baker speak?
Dr. Baker and their clinical team can communicate with patients in the following languages:
English
Spanish
What conditions does Dr. Baker treat?
As a Clinical Geneticist, Dr. Baker 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. Baker. 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
- Tyrosinemia
- Argininosuccinic Aciduria
- Acidosis
- Metabolic Disorder
- Tetrahydrobiopterin deficiency
- Argininosuccinic aciduria
- Hyperphenylalaninemia
- Phenylalanine Metabolism Disorder
- Phenylketonuria (PKU)
- Tyrosine Metabolism Disorder
- Tyrosinosis
- Argininosuccinic Acid Lyase Deficiency
- ASA Lyase Deficiency
- Acidic Blood
- High Acidity in Body
ICD-10 Codes:
- E701: Other hyperphenylalaninemias
- E7021: Tyrosinemia
- E7222: Arginosuccinic aciduria
- E8720: Acidosis, unspecified
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:
- Abnormal Newborn Screening Results
- Newborn Screening
- Positive newborn screen
- Failed newborn screening
- Newborn test abnormalities
ICD-10 Codes:
- P099: Abnormal findings on neonatal screening, unspecified
Also known as:
- Other Specific Birth Defects
- Birth Defects Causing Overgrowth
- Birth Defects
- Rare Congenital Anomalies
- Uncommon Birth Malformations
- Overgrowth Syndromes
- Congenital Gigantism
ICD-10 Codes:
- Q898: Other specified congenital malformations
- Q873: Congenital malformation syndromes involving early overgrowth
Also known as:
- Autism
- Autism Spectrum Disorder
- Classic Autism', 'Kanner's Syndrome
- Severe Autism
ICD-10 Codes:
- F840: Autistic disorder
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:
- Chromosomal Abnormality
- Genetic Disorder
- Genetic Chromosome Disorder
- Chromosome Problem
- Aneuploidy
ICD-10 Codes:
- Q999: Chromosomal abnormality, unspecified
Also known as:
- Failure to Thrive in Children
- Growth Disorder
- Poor growth in children
- Childhood growth problems
- Infant growth failure
ICD-10 Codes:
- R6251: Failure to thrive (child)
Also known as:
- Rhabdomyolysis
- Muscle Disorder
- Muscle Breakdown
- Acute Muscle Injury
- Myoglobinuria
ICD-10 Codes:
- M6282: Rhabdomyolysis
Also known as:
- Galactosemia
- Carbohydrate Metabolism Disorder
- Galactose intolerance
- Galactose metabolism disorder
- GALT deficiency
ICD-10 Codes:
- E7421: Galactosemia
Also known as:
- Osteogenesis Imperfecta
- Dentinogenesis imperfecta
- Brittle bone disease
- OI
- Fragile bones
ICD-10 Codes:
- Q780: Osteogenesis imperfecta
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:
- 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:
- 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:
- Other Specific Abnormal Blood Chemistry Results
- Blood
- Specified Blood Chemistry Imbalance
- Unusual Blood Chemistry Findings
- Specific Blood Panel Abnormalities
ICD-10 Codes:
- R7989: Other specified abnormal findings of blood chemistry
Also known as:
- Low Blood Sugar
- Hypoglycemia
- Low Blood Glucose (Hypoglycemia)
- Blood Sugar Drop
- Sugar Crash
ICD-10 Codes:
- E162: Hypoglycemia, unspecified
Which procedures does Dr. Baker perform as a Clinical Geneticist?
As a Clinical Geneticist, procedures performed by a Dr. Craig Baker may include:
- Biochemical Genetics Consultation
- Biochemical Genetics Follow Up
- Enzyme Replacement Therapy
- Genetic Testing
- Metabolic Assessment and Management
For detailed information, please contact Dr. Baker's office.
Does Dr. Baker accept my insurance?
Dr. Baker accepts most major insurance plans. Important: Please call our office at (402) 559-6403 before your appointment to verify that your specific plan and network are accepted.
What insurance plans does Dr. Baker accept in Omaha, NE?
Dr. Baker in Omaha, NE accepts plans from many carriers. While this list is updated regularly, it is not a guarantee of coverage.
Top Insurances
All Other Third Party
BCBS Unspecified
Blue Cross and Blue Shield of Nebraska
Centene
Department of Defense / Tricare
Elevance Health Inc. (formerly Anthem)
Federal Employee Program
Medicare
Molina
UnitedHealthcare
View All Insurances
Where is Dr. Baker's office located?
What is Dr. Baker's NPI number?An National Provider Identifier (NPI) is a unique ID number that identifies doctors and healthcare providers nationwide.
Dr. Baker's National Provider Identifier (NPI) number is 1003203779.
What common questions do patients ask about Dr. Baker?
Here are answers to patients Frequently Asked Questions (FAQ’s) about Dr. Baker
What is Dr. Craig Baker's specialty?
Dr. Baker is a Clinical Geneticist near Omaha, NE. A clinical geneticist is adept at offering thorough diagnostic, management, and counseling services for genetic disorders. Contact Dr. Baker to book an appointment today.
Is this Dr. Craig Baker affiliated with a ranked Castle Connolly Top Hospital?
No, Baker is not affiliated with a Castle Connolly Top Hospital, but is affiliated with the following hospitals: Childrens Nebraska. 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 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 Craig Baker accepting new patients in Omaha, NE?
Yes, Dr. Craig Baker is accepting new patients at this time.
Does Dr. Craig Baker offer online booking?
Please contact Dr. Baker's office at (402) 559-6403 for information about online booking, telehealth, or to schedule an appointment.
How can I make an appointment with Craig Baker?
Please contact Dr. Baker's office at (402) 559-6403 for information regarding telehealth appointment availability or for scheduling assistance.
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