The 20 Best Fabry Disease Doctors Near Me in san anselmo, CA

Find the Top Fabry Disease Experts and Specialists

Last Updated: 09/26/2026

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MediFind found 5 doctor with experience in Fabry Disease near san anselmo, CA. Of these, 3 are Experienced and 2 are Advanced.

Location
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5 providers found
    Experienced in Fabry Disease
    Internal Medicine
    Experienced in Fabry Disease
    Internal Medicine

    DBT Psychology Center Of Marin PC

    895 Sir Francis Drake Blvd, 
    San Anselmo, CA 
     (0.4 miles away)
    Languages Spoken:
    English
    Offers Telehealth

    David Ogden is a primary care provider, practicing in Internal Medicine in San Anselmo, California. Dr. Ogden is rated as an Experienced provider by MediFind in the treatment of Fabry Disease. His clinical expertise encompasses Chronic Cough, Fainting, Maturity Onset Diabetes of the Young, and Vertigo.

    Advanced in Fabry Disease
    Internal Medicine
    Advanced in Fabry Disease
    Internal Medicine

    Office

    444 Laverne Ave, 
    Mill Valley, CA 
     (5.3 miles away)
    Languages Spoken:
    English

    David Kirn is a primary care provider, practicing in Internal Medicine in Mill Valley, California. Dr. Kirn is rated as an Advanced provider by MediFind in the treatment of Fabry Disease. He is also highly rated in 2 other conditions, according to our data. His clinical expertise encompasses Fabry Disease, Liver Cancer, Cystic Fibrosis, and Colorectal Cancer.

    Advanced in Fabry Disease
    Medical Genetics | Pediatrics
    Advanced in Fabry Disease
    Medical Genetics | Pediatrics
    Referral may be required

    University Of California San Francisco

    2330 Post St, 
    San Francisco, CA 
     (14.7 miles away)
    Languages Spoken:
    English, Mandarin, Spanish
    Accepting New Patients
    Offers Telehealth

    Irene Chang is a Medical Genetics specialist and a Pediatrics provider practicing medicine in San Francisco, California. Dr. Chang is rated as an Advanced provider by MediFind in the treatment of Fabry Disease. She is also highly rated in 5 other conditions, according to our data. Her clinical expertise encompasses Biotinidase Deficiency, MPI-CDG, Adrenoleukodystrophy (ALD), and Carnitine-Acylcarnitine Translocase Deficiency. Dr. Chang is currently accepting new patients.

    Learn about our expert tiers
    Experienced in Fabry Disease
    Medical Genetics | Pediatrics
    Experienced in Fabry Disease
    Medical Genetics | Pediatrics
    Referral may be required

    University Of California San Francisco

    2330 Post St, 
    San Francisco, CA 
     (14.7 miles away)
    Languages Spoken:
    English, Arabic, French
    Accepting New Patients
    Offers Telehealth

    Hind Al Saif is a Medical Genetics specialist and a Pediatrics provider practicing medicine in San Francisco, California. Dr. Al Saif is rated as an Experienced provider by MediFind in the treatment of Fabry Disease. She is also highly rated in 3 other conditions, according to our data. Her clinical expertise encompasses Pompe Disease, Danon Disease, Oculocutaneous Albinism, and Phenylketonuria (PKU). Dr. Al Saif is currently accepting new patients.

    Experienced in Fabry Disease
    Medical Genetics | Pediatrics
    Experienced in Fabry Disease
    Medical Genetics | Pediatrics
    Referral may be required

    University Of California San Francisco

    2330 Post St, 
    San Francisco, CA 
     (14.7 miles away)
    Languages Spoken:
    English

    Jose Camacho is a Medical Genetics specialist and a Pediatrics provider practicing medicine in San Francisco, California. Dr. Camacho is rated as an Experienced provider by MediFind in the treatment of Fabry Disease. His clinical expertise encompasses Fabry Disease, Megalencephalic Leukoencephalopathy with Subcortical Cysts, and Multiple Sulfatase Deficiency.

    Showing 1-5 of 5

    Last Updated: 09/26/2026

    What is the definition of Fabry Disease?

    Fabry disease is an inherited disorder that results from the buildup of a type of fat, called globotriaosylceramide, in the body's cells. Beginning in childhood, this buildup causes signs and symptoms that affect many parts of the body. Characteristic features of Fabry disease include episodes of pain, particularly in the hands and feet (acroparesthesias); clusters of small, dark red spots on the skin called angiokeratomas; a decreased ability to sweat (hypohidrosis); cloudiness or streaks in the front part of the eye (corneal opacity or corneal verticillata); problems with the gastrointestinal system; ringing in the ears (tinnitus); and hearing loss. Additional signs and symptoms are possible, which can vary among affected individuals.

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