Who is Dr. Beltran Carranza, Clinical Geneticist in Wichita, KS?
What languages does Dr. Beltran Carranza speak?
Dr. Beltran Carranza and their clinical team can communicate with patients in the following languages:
- English
- Spanish
What conditions does a Clinical Geneticist like Dr. Beltran Carranza typically treat?
As a Clinical Geneticist, Dr. Beltran Carranza 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. Beltran Carranza. 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. Learn more about our claims-based healthcare methodology.
Also known as:
- Phenylketonuria (PKU)
- Phenylketonuria
- PKU
- Følling's Disease
- Phenylalanine Hydroxylase Deficiency
ICD-10 Codes:
- E700: Classical phenylketonuria
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 Developmental Disabilities
- Developmental Disabilities
- Atypical psychological development
- Unspecified developmental disorder
ICD-10 Codes:
- F88: Other disorders of psychological development
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:
- 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:
- Autism
- Autism Spectrum Disorder
- Classic Autism
- Kanner's Syndrome
- Severe Autism
ICD-10 Codes:
- F840: Autistic disorder
Also known as:
- Abnormal Newborn Screening for Metabolic Disorder
- Newborn metabolic screening issue
- Inborn errors of metabolism screening
- Positive newborn metabolic screen
ICD-10 Codes:
- P091: Abnormal findings on neonatal screening for inborn errors of metabolism
Also known as:
- Medium-Chain Acyl-CoA Dehydrogenase Deficiency
- Lipid Metabolism Disorder
- Medium-chain acyl-CoA dehydrogenase deficiency
- MCAD Deficiency
- Medium-Chain Fatty Acid Oxidation Disorder
- MCADD
ICD-10 Codes:
- E71311: Medium chain acyl CoA dehydrogenase deficiency
What procedures does a Clinical Geneticist like Dr. Beltran Carranza typically perform?
As a Clinical Geneticist, procedures performed by Dr. Elizabeth Beltran Carranza may include:
- Biochemical Genetics Consultation
- Biochemical Genetics Follow Up
- Enzyme Replacement Therapy
- Genetic Testing
- Metabolic Assessment and Management
Please contact Dr. Beltran Carranza's office directly to confirm care for your specific procedure, for more information, or to schedule a consultation.
Does Dr. Beltran Carranza accept my insurance?
Dr. Beltran Carranza accepts most major insurance plans. Important: Please call our office at (316) 293-2611 before your appointment to verify that your specific plan and network are accepted.
What insurance plans does Dr. Beltran Carranza accept in Wichita, KS?
Dr. Beltran Carranza in Wichita, KS accepts plans from many carriers. While this list is updated regularly, it is not a guarantee of coverage.
Top Insurances
Allied Benefit Systems
CVS Health (formerly Aetna)
View All Insurances
Where is Dr. Beltran Carranza's office located?
Dr. Elizabeth Beltran Carranza's Primary Practice
2600 N Woodlawn Blvd
Wichita, KS 67220
(316) 293-2611
What is Dr. Beltran Carranza's NPI number?A National Provider Identifier (NPI) is a unique ID number that identifies doctors and healthcare providers nationwide.
Dr. Beltran Carranza's National Provider Identifier (NPI) number is 1861623985.
What common questions do patients ask about Dr. Beltran Carranza?
Here are answers to patients Frequently Asked Questions (FAQ’s) about Dr. Beltran Carranza