The 20 Best Inborn Amino Acid Metabolism Disorder Doctors Near Me in pittsburg, CA

Find the Top Inborn Amino Acid Metabolism Disorder Experts and Specialists

Last Updated: 09/26/2026

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MediFind found 2 doctor with experience in Inborn Amino Acid Metabolism Disorder near pittsburg, CA. Of these, 2 are Experienced.

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2 providers found
    Experienced in Inborn Amino Acid Metabolism Disorder

    Dr. Oliver Z. Graham
    Internal Medicine
    Experienced in Inborn Amino Acid Metabolism Disorder

    Dr. Oliver Z. Graham
    Internal Medicine

    Contra Costa County

    2311 Loveridge Rd, 
    Pittsburg, CA 
     (1.7 miles away)
    800-495-8885
    Languages Spoken:
    English
    See accepted insurances

    Oliver Graham is a primary care provider, practicing in Internal Medicine in Pittsburg, California. Dr. Graham is rated as an Experienced provider by MediFind in the treatment of Inborn Amino Acid Metabolism Disorder. His clinical expertise encompasses Nephrogenic Diabetes Insipidus, IPEX Syndrome, Autoimmune Polyendocrinopathy-Candidiasis-Ectodermal Dystrophy (APECED), Endoscopy, and Gastrostomy.

    Experienced in Inborn Amino Acid Metabolism Disorder

    Dr. Edsil A. De Ocampo
    Internal Medicine
    Experienced in Inborn Amino Acid Metabolism Disorder

    Dr. Edsil A. De Ocampo
    Internal Medicine

    Office

    1450 Treat Blvd Ste 350, 
    Walnut Creek, CA 
     (11.5 miles away)
    925-275-9200
    Languages Spoken:
    English
    See accepted insurances

    Edsil De Ocampo is a primary care provider, practicing in Internal Medicine in Walnut Creek, California. Dr. De Ocampo is rated as an Experienced provider by MediFind in the treatment of Inborn Amino Acid Metabolism Disorder. He is also highly rated in 19 other conditions, according to our data. His clinical expertise encompasses Sepsis, Peptic Ulcer, Necrosis, Gastrostomy, and Ureteroscopy.

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    Last Updated: 09/26/2026

    What is the definition of Inborn Amino Acid Metabolism Disorder?

    Inborn amino acid metabolism disorder is a term used to describe genetic conditions such as phenylketonuria (PKU), maple syrup disease, fructose intolerance, and galactosemia. In inborn amino acid metabolism disorders, the body does not break down amino acids properly, which are chemicals that help to form proteins. This inability to break down amino acids causes a build up of harmful substances in the body.

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