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Dr. Terry Kho, MD

Seattle, WA

Accepting patients

    Who is Dr. Kho, Medical Biochemical Geneticist in Seattle, WA?

    Dr. Terry Kho, MD is a Medical Biochemical Geneticist, who primarily practices in Seattle, WA with 2 additional practice locations. She is board certified. Dr. Kho is fluent in English, and is currently seeing new patients. Dr. Kho’s practice accepts Cigna, Kaiser Permanente, Medicare, UnitedHealthcare and other major insurance plans. To book an appointment or to confirm insurance options, please call Dr. Kho’s office at (206) 520-5000.

    What languages does Dr. Kho speak?

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

    • English

    What conditions does Dr. Kho treat?

    As a Medical Biochemical Geneticist, Dr. Kho 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. Kho. 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:

    • Ornithine Metabolism Disorder
    • Lysine and Hydroxylysine Metabolism Disorder
    • Amino Acid Metabolism Disorder
    • Ornithine translocase deficiency
    • Hyperlysinemia
    • Ornithine Translocase Deficiency
    • Hyperornithinemia
    • Ornithine Processing Problems
    • Lysine Processing Problems
    • Genetic Lysine Disorder

    ICD-10 Codes:

    • E724: Disorders of ornithine metabolism
    • E723: Disorders of lysine and hydroxylysine metabolism

    Also known as:

    • High Phenylalanine Levels
    • Pyruvate Metabolism Disorder
    • Urea Cycle Disorder
    • Branched-Chain Amino Acid Metabolism
    • Metabolic Disorder
    • Tetrahydrobiopterin deficiency
    • Pyruvate carboxylase deficiency
    • Hyperphenylalaninemia
    • Phenylalanine Metabolism Disorder
    • Phenylketonuria (PKU)
    • Gluconeogenesis disorder
    • Pyruvate dehydrogenase deficiency
    • UCD
    • Urea Cycle Enzyme Problem
    • Ammonia Processing Disorder
    • Branched-Chain Amino Acid Disorders
    • Branched-Chain Amino Acid Metabolism Condition

    ICD-10 Codes:

    • E701: Other hyperphenylalaninemias
    • E744: Disorders of pyruvate metabolism and gluconeogenesis
    • E7220: Disorder of urea cycle metabolism, unspecified
    • E7119: Other disorders of branched-chain amino-acid metabolism

    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:

    • 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:

    • X-linked Adrenoleukodystrophy
    • Leukodystrophies
    • X-linked adrenoleukodystrophy
    • ALD
    • Adrenoleukodystrophy

    ICD-10 Codes:

    • E71529: X-linked adrenoleukodystrophy, unspecified type

    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:

    • 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:

    • 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:

    • 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:

    • 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:

    • 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:

    • Genetic Counseling
    • Genetic risk assessment
    • Hereditary counseling
    • DNA counseling

    ICD-10 Codes:

    • Z7183: Encounter for nonprocreative genetic counseling

    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:

    • Low Blood Sugar
    • Hypoglycemia
    • Low Blood Glucose (Hypoglycemia)
    • Blood Sugar Drop
    • Sugar Crash

    ICD-10 Codes:

    • E162: Hypoglycemia, unspecified

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

    As a Medical Biochemical Geneticist, procedures performed by a Dr. Terry Kho may include:

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

    Does Dr. Kho accept my insurance?

    Dr. Kho accepts most major insurance plans. Important: Please call our office at (206) 520-5000 before your appointment to verify that your specific plan and network are accepted.

    What insurance plans does Dr. Kho accept in Seattle, WA?

    Dr. Kho in Seattle, WA accepts plans from many carriers. While this list is updated regularly, it is not a guarantee of coverage.

    Top Insurances

    • Boeing

    • Cambia (Regence)

    • Community Health Plan of Washington

    • CVS Health (formerly Aetna)

    • Elevance Health Inc. (formerly Anthem)

    • Kaiser Permanente

    • Molina

    • Premera Blue Cross

    • State of Washington

    • UnitedHealthcare

    View All Insurances

    Where is Dr. Kho's office located?

    Dr. Terry Kho's Primary Practice

    4800 Sand Point Way NE

    Seattle, WA 98105

    (206) 520-5000

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    Dr. Terry Kho's Practice 2

    1959 NE Pacific St

    Seattle, WA 98195

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    Dr. Terry Kho's Practice 3

    3181 SW Sam Jackson Park Rd

    Portland, OR 97239

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

    Dr. Kho's National Provider Identifier (NPI) number is 1760916860.

    What common questions do patients ask about Dr. Kho?

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

    What is Dr. Terry Kho's specialty?

    Dr. Kho is a Medical Biochemical Geneticist near Seattle, WA. 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. Kho to book an appointment today.

    Is this Dr. Terry Kho affiliated with a ranked Castle Connolly Top Hospital?

    No, Kho is not affiliated with a Castle Connolly Top Hospital, but is affiliated with the following hospitals: Seattle Childrens Hospital, Shriners Childrens Spokane. 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 Terry Kho accepting new patients in Seattle, WA?

    Yes, Dr. Terry Kho is accepting new patients at this time.

    Does Dr. Terry Kho offer online booking?

    Please contact Dr. Kho's office at (206) 520-5000 for information about online booking, telehealth, or to schedule an appointment.

    How can I make an appointment with Terry Kho?

    Please contact Dr. Kho's office at (206) 520-5000 for information regarding telehealth appointment availability or for scheduling assistance.

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