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Dr. Luis Umana, MD

Dallas, TX

Accepting patients

    Who is Dr. Umana, Medical Biochemical Geneticist in Dallas, TX?

    Dr. Luis Umana, MD is a Medical Biochemical Geneticist, who primarily practices in Dallas, TX with 2 additional practice locations. He is board certified by the American Board of Pediatrics. Dr. Umana is fluent in English and Spanish, and is currently seeing new patients. Dr. Umana’s practice accepts UnitedHealthcare and other major insurance plans. To book an appointment or to confirm insurance options, please call Dr. Umana’s office at (214) 456-9093.

    Where did Dr. Umana go to medical school and complete their residency?

    • Medical School: Harvard Medical School, Boston, Massachusetts

    Is Dr. Umana board certified in Medical Biochemical Geneticist?

    Yes, Dr. Luis Umana, MD is board certified by the American Board of Pediatrics

    What languages does Dr. Umana speak?

    Dr. Umana and their clinical team can communicate with patients in the following languages:

    • English

    • Spanish

    What conditions does Dr. Umana treat?

    As a Medical Biochemical Geneticist, Dr. Umana 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. Umana. 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
    • Maple Syrup Urine Disease
    • Argininosuccinic Aciduria
    • Primary Carnitine Deficiency
    • Biotinidase Deficiency
    • Citrullinemia
    • Branched-Chain Amino Acid Metabolism
    • Metabolic Disorder
    • Tetrahydrobiopterin deficiency
    • Maple syrup urine disease
    • Argininosuccinic aciduria
    • Primary carnitine deficiency
    • Immune System and Disorder
    • Biotinidase deficiency
    • Hyperphenylalaninemia
    • Phenylalanine Metabolism Disorder
    • Phenylketonuria (PKU)
    • MSUD
    • Branched-Chain Ketoaciduria
    • Argininosuccinic Acid Lyase Deficiency
    • ASA Lyase Deficiency
    • Systemic Primary Carnitine Deficiency
    • Carnitine Uptake Defect
    • BTD deficiency
    • Biotin deficiency
    • Genetic metabolic disorder
    • Urea Cycle Disorder Type II
    • Citrulline Disorder
    • Branched-Chain Amino Acid Disorders
    • Branched-Chain Amino Acid Metabolism Condition

    ICD-10 Codes:

    • E701: Other hyperphenylalaninemias
    • E710: Maple-syrup-urine disease
    • E7222: Arginosuccinic aciduria
    • E7141: Primary carnitine deficiency
    • D81810: Biotinidase deficiency
    • E7223: Citrullinemia
    • E7119: Other disorders of branched-chain amino-acid metabolism

    Also known as:

    • Very Long-Chain Acyl-CoA Dehydrogenase Deficiency
    • Medium-Chain Acyl-CoA Dehydrogenase Deficiency
    • Lipid Metabolism Disorder
    • Very long-chain acyl-CoA dehydrogenase deficiency
    • Medium-chain acyl-CoA dehydrogenase deficiency
    • VLCAD Deficiency
    • Long-Chain Fatty Acid Oxidation Disorder
    • VLCADD
    • MCAD Deficiency
    • Medium-Chain Fatty Acid Oxidation Disorder
    • MCADD

    ICD-10 Codes:

    • E71310: Long chain/very long chain acyl CoA dehydrogenase deficiency
    • E71311: Medium chain acyl CoA dehydrogenase deficiency

    Also known as:

    • Methylmalonic Acidemia
    • Metabolic Disorder
    • Methylmalonic acidemia
    • MMA
    • Methylmalonic Aciduria
    • Methylmalonic Acidopathy

    ICD-10 Codes:

    • E71120: Methylmalonic acidemia

    Also known as:

    • Mucopolysaccharidosis Type II
    • Sanfilippo Syndrome
    • Carbohydrate Metabolism Disorder
    • Mucopolysaccharidosis type II
    • Mucopolysaccharidosis type III
    • MPS II
    • Hunter syndrome
    • MPS III
    • Sanfilippo disease

    ICD-10 Codes:

    • E761: Mucopolysaccharidosis, type II
    • E7622: Sanfilippo mucopolysaccharidoses

    Also known as:

    • Multiple Birth Defects
    • Other Genetic Syndrome
    • Birth Defects
    • Complex congenital anomalies
    • Multiple congenital anomalies
    • Syndromic birth defects
    • Rare Birth Defect Syndromes
    • Uncommon Congenital Syndromes

    ICD-10 Codes:

    • Q897: Multiple congenital malformations, not elsewhere classified
    • Q8789: Other specified congenital malformation syndromes, not elsewhere classified

    Also known as:

    • Other Specific B Vitamin Deficiency
    • B Vitamins
    • Malnutrition
    • Specific B Vitamin Shortage
    • Less Common B Vitamin Deficiency
    • Rare B Vitamin Deficiency

    ICD-10 Codes:

    • E538: Deficiency of other specified B group vitamins

    Also known as:

    • Lysine and Hydroxylysine Metabolism Disorder
    • Amino Acid Metabolism Disorder
    • Hyperlysinemia
    • Lysine Processing Problems
    • Genetic Lysine Disorder

    ICD-10 Codes:

    • E723: Disorders of lysine and hydroxylysine metabolism

    Also known as:

    • Dependence on Ventilator
    • Respirator Dependence
    • Breathing Machine Reliance
    • Long-term Ventilation

    ICD-10 Codes:

    • Z9911: Dependence on respirator [ventilator] status

    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:

    • Glycogen Storage Disease
    • Carbohydrate Metabolism Disorder
    • Glycogen storage disease type 0
    • Glycogen storage disease type IV
    • Glycogen storage disease type VI
    • GSD
    • Glycogenosis
    • Glycogen Storage Disease Type 0
    • Glycogen Storage Disease Type IV

    ICD-10 Codes:

    • E7409: Other glycogen storage disease

    Also known as:

    • Galactose Metabolism Disorder
    • Carbohydrate Metabolism Disorder
    • Galactosemia
    • Galactose Processing Problems
    • Genetic Galactose Disorder

    ICD-10 Codes:

    • E7429: Other disorders of galactose metabolism

    Which procedures does Dr. Umana perform as a Medical Biochemical Geneticist?

    As a Medical Biochemical Geneticist, procedures performed by a Dr. Luis Umana may include:

    For detailed information, please contact Dr. Umana's office.

    Does Dr. Umana accept my insurance?

    Dr. Umana accepts most major insurance plans. Important: Please call our office at (214) 456-9093 before your appointment to verify that your specific plan and network are accepted.

    What insurance plans does Dr. Umana accept in Dallas, TX?

    Dr. Umana in Dallas, TX accepts plans from many carriers. While this list is updated regularly, it is not a guarantee of coverage.

    Top Insurances

    • All Other Third Party

    • Baylor Scott & White Health

    • Centene

    • Cook Children's

    • CVS Health (formerly Aetna)

    • Health Care Service Corporation (HCSC)

    • Molina

    • Parkland Community Health Plan

    • State of Texas

    • UnitedHealthcare

    View All Insurances

    Where is Dr. Umana's office located?

    Dr. Luis Umana's Primary Practice

    5323 Harry Hines Blvd

    Dallas, TX 75390

    (214) 456-9093

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    Dr. Luis Umana's Practice 2

    7601 Preston Rd

    Plano, TX 75024

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    Dr. Luis Umana's Practice 3

    1935 Medical District Dr

    Dallas, TX 75235

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    What is Dr. Umana's NPI number?An National Provider Identifier (NPI) is a unique ID number that identifies doctors and healthcare providers nationwide.

    Dr. Umana's National Provider Identifier (NPI) number is 1710145362.

    What common questions do patients ask about Dr. Umana?

    Here are answers to patients Frequently Asked Questions (FAQ’s) about Dr. Umana

    What is Dr. Luis Umana's specialty?

    Dr. Umana is a Medical Biochemical Geneticist near Dallas, TX. A medical biochemical geneticist is an expert in diagnosing, evaluating, preventing, and treating biochemical genetic disorders, recognized as inborn errors of metabolism that can arise at any age. Their training does not provide the necessary skills to manage a clinical laboratory. Contact Dr. Umana to book an appointment today.

    Is this Dr. Luis Umana affiliated with a ranked Castle Connolly Top Hospital?

    No, Umana is not affiliated with a Castle Connolly Top Hospital, but is affiliated with the following hospitals: Childrens Medical Center Dallas, Parkland Health. 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 Medical Biochemical Geneticist?

    Explore Medical 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 Luis Umana accepting new patients in Dallas, TX?

    Yes, Dr. Luis Umana is accepting new patients at this time.

    Does Dr. Luis Umana offer online booking?

    Please contact Dr. Umana's office at (214) 456-9093 for information about online booking, telehealth, or to schedule an appointment.

    How can I make an appointment with Luis Umana?

    Please contact Dr. Umana's office at (214) 456-9093 for information regarding telehealth appointment availability or for scheduling assistance.

    Which board certifications does Dr. Luis Umana have?

    Dr. Luis Umana is certified by the American Board of Pediatrics.

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