Photo of Ora K. Gordon, MD

Ora K. Gordon, MD

Accepting New Patients
Offers Video Visits
20929 Hawthorne Boulevard
Torrance, CA 90503
2283.2 miles away
Medical Groups & Affiliations
Providence Specialty Medical Group
Speaks: Spanish and English
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Providence Women's Imaging Center - Torrance

20929 Hawthorne Boulevard, Torrance, CA 90503

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About Ora K. Gordon

Dr. Gordon is the medical director of the Providence Center for Clinical Genetics and Genomics, and the Department of Integrative Medicine at the Roy and Patricia Disney Family Cancer Center. She is one of few medical geneticists in the Los Angeles area. Before joining Providence, Dr. Gordon spent 13 years at Cedars-Sinai Medical Center as director of the GenRISK Adult Genetics Program, co-director of the Gilda Radner Hereditary Cancer Program and training director for the UCLA Medical Genetics Residency Program. A nationally recognized expert in hereditary cancer, Dr. Gordon is co-author of an award-winning book on understanding and managing breast and ovarian cancer risk, “Positive Results: Making the Best Decisions When You’re at High Risk for Breast or Ovarian Cancer.” Dr. Gordon’s primary research interests involve the prevention of breast cancer. She has been involved in numerous clinical trials for cancer prevention. Dr. Gordon is board-certified in both internal medicine and medical genetics, and she serves as an associate professor of medicine at the UCLA David Geffen School of Medicine. Passionate about a holistic approach to health and disease prevention, Dr. Gordon has also completed a fellowship in integrative medicine through the University of Arizona Center for Integrative Medicine.

Medical School

University of California
1995

Internship

UCLA Medical Center
1996

Residency

UCLA Medical Center
1999

Fellowship

Cedars Sinai Medical Center
2001

Fellowship

University of Arizona
2016

Board Certifications
  • American Board of Medical Genetics and Genomics, Clinical Genetics (MD)
Providence Women's Imaging Center - Torrance
20929 Hawthorne Boulevard
Torrance, CA 90503

Roy & Patricia Disney Family Cancer Center
181 South Buena Vista Street, Floor 1
Burbank, CA 91505

Providence Saint John's Cancer Institute
2200 Santa Monica Boulevard
Santa Monica, CA 90404

Providence Clinical Genetics and Genomics Program - Burbank
181 South Buena Vista Street, Suite 110
Burbank, CA 91505

Providence Clinical Genetics and Genomics Program - Saint John's
2200 Santa Monica Boulevard
Santa Monica, CA 90404

Providence Clinical Genetics and Genomics Program - Mission Hills
15031 Rinaldi Street
Mission Hills, CA 91345

Medical Groups & Affiliations
Providence Specialty Medical Group

Affiliated Locations
Saint John’s Health Center Cancer Clinic – Santa Monica
Providence Little Company of Mary Medical Center Torrance
Providence Saint John's Health Center
Providence Saint Joseph Medical Center

Clinical Interests

  • 25-Hydroxyvitamin D Test
  • Abdominal Cramps
  • Abdominal Hernia
  • Abdominal Mass
  • Abdominal Pain
  • Abdominal Trauma
  • Abdominal Wall Defect
  • Abnormal Bowel Movement
  • Abnormal Breathing
  • Abnormal Newborn Screening
  • Abnormal Pap Smear
  • Abnormal Stool
  • Abnormal Urine Odor
  • Abnormalities Of The Arms
  • Abnormalities Of The Feet
  • Abnormalities Of The Hands
  • Abortion Information
  • Abrasion
  • Abusive Head Trauma
  • Achilles Tendon Disorders
  • Achondroplasia
  • Acrocephalosyndactyly
  • Adrenoleukodystrophy (Ald)
  • Aicardi Syndrome
  • Alagille Syndrome
  • Albinism
  • Alpha 1 Antitrypsin Deficiency
  • Alport Syndrome
  • Anal Stenosis
  • Androgen Insensitivity
  • Angelman Syndrome
  • Aniridia
  • Apc Gene
  • Arteriovenous Malformation (Avm)
  • Autism
  • Axin2 Gene
  • Bap1 Gene
  • Bard1 Gene
  • Barth Syndrome
  • Becker Muscular Dystrophy
  • Beckwith Wiedemann Syndrome
  • Bethlem Myopathy
  • Blepharophimosis
  • Blood Disorders
  • Blue Diaper Syndrome
  • Bmpr1a Gene
  • Bohring Opitz Syndrome (Bos)
  • Bone Disorders
  • Brca
  • Breast Cancer
  • Breast Cancer Genetic Testing
  • Breast Cancer Genetics
  • Brugada Syndrome
  • C Syndrome
  • Cafe Au Lait Spots
  • Cancer Genomics
  • Cancer Predisposition Syndromes
  • Cardiac Genetics
  • Cardiomyopathy
  • Carnitine Deficiency
  • Carnitine Disorders
  • Cataract
  • Cdh13 Gene
  • Cdk4 Gene
  • Cdkl5 Mutation
  • Cdkn2a Gene
  • Central Core Disease
  • Cerebellar Anomalies
  • Cerebral Anomalies
  • Cerebral Palsy
  • Charcot Marie Tooth Disease
  • Charge Syndrome
  • Checkpoint Kinase 2
  • Childhood Obesity
  • Chromosomal Microarray Analysis
  • Chromosome Abnormality
  • Chromosome Duplication
  • Chronic Granulomatous Disorder
  • Cirrhosis
  • Cleidocranial Dysostosis
  • Coloboma
  • Congenital Adrenal Hyperplasia
  • Congenital Diaphragmatic Hernia (Cdh)
  • Congenital Esophageal Atresia
  • Congenital Generalized Lipodystrophy
  • Congenital Heart Disease
  • Congenital Hyperinsulinism
  • Congenital Limb Defects
  • Connective Tissue Disorder
  • Cornelia De Lange Syndrome
  • Costello Syndrome
  • Cutis Aplasia
  • Cyp2c19 Mutation
  • Cyp2d6 Mutation
  • Cystic Fibrosis
  • Cystic Fibrosis Gene Carrier
  • Deafness
  • Deficiency Of Interleukin1receptor Antagonist
  • Dejerine Sottas Disease
  • Denys Drash Syndrome (Dds)
  • Developmental Delay
  • Developmental Regression
  • Diabetes Mellitus
  • Diaphragmatic Hernia
  • Dicer1 Gene
  • Digeorge Syndrome
  • Disorders Of Sexual Differentiation
  • Distal Muscular Dystrophy
  • Distal Myopathy
  • Down Syndrome
  • Duane Syndrome
  • Duchenne Muscular Dystrophy
  • Dup15q Syndrome
  • Dystonia
  • Ectodermal Dysplasias
  • Edema
  • Ehlers Danlos
  • Ellis-Van Creveld Syndrome
  • Epcam Gene
  • Epilepsy
  • Esophageal Atresia
  • Exercise Intolerance
  • Facial Asymmetry
  • Facioscapulohumeral Muscular Dystrophy
  • Failure To Thrive
  • Familial Medullary Thyroid Cancer (Fmtc)
  • Familial Partial Lipodystrophy
  • Familial Spinal Muscle Atrophy
  • Family History Of Autism
  • Family History Of Birth Defects
  • Family History Of Cancer
  • Family History Of Colon Cancer
  • Family History Of Colon Polyps
  • Family History Of Glaucoma
  • Fatal Familial Insomnia (Ffi)
  • Fetal Alcohol Syndrome
  • Fetal Growth Restriction
  • Fish Cancer Test
  • Flcn Gene
  • Fracture
  • Fragile X Syndrome
  • Frasier Syndrome
  • Galnt12 Gene
  • Gaucher Disease
  • Genetic Causes Of Vascular Malformations
  • Genetic Counseling
  • Genetic Disorders
  • Genetic Dystonia
  • Genetic Testing Colon Cancer
  • Genetic Testing Ovarian Cancer
  • Glaucoma
  • Glaucoma Of Childhood
  • Glucose Galactose Malabsorption (Ggm)
  • Glycogen Storage Disease
  • Gorlin Syndrome
  • Grem1 Gene
  • Grin Mutation
  • Hearing Loss
  • Hearing Loss (Genetic)
  • Hemihypertrophy
  • Hemochromatosis
  • Hemoglobinopathies
  • Hemophagocytic Lymphohistiocytosis
  • Hemophilia
  • Hemophilia Inhibitors
  • Her2 Positive Breast Cancer
  • Hereditary Hemorrhagic Telangiectasia
  • Hereditary Polyposis
  • Hereditary Retinoblastoma
  • Hereditary Spastic Paraplegia
  • Hermansky Pudlak Syndrome
  • Hirschsprung's Disease
  • Holt-Oram Syndrome
  • Hormone Receptor Positive Breast Cancer
  • Hoxb13 Gene
  • Hunter Syndrome
  • Hurler Syndrome
  • Hydrocephalus
  • Hypermobility Syndrome
  • Hypertrophic Cardiomyopathy
  • Hypoglycemia
  • Hypophosphatasia
  • Hypospadias
  • Hypotonia
  • Immune Deficiency
  • Inborn Errors Of Metabolism
  • Infertility
  • Intellectual Disabilities
  • Intestinal Atresia
  • Ipex Syndrome
  • Kabuki Syndrome
  • Kcnb1 Mutation
  • Kearns Sayre Syndrome
  • Kidney Dysplasia
  • Kit Gene
  • Klinefelter Syndrome
  • Klippel Trenaunay Syndrome
  • Learning Disabilities
  • Learning Disorders
  • Leber Hereditary Optic Neuropathy
  • Leigh's Disease
  • Leukodystrophy
  • Li Fraumeni Syndrome
  • Lissencephaly
  • Long Qt Syndrome
  • Lynch Syndrome
  • Lysosomal Diseases
  • Macrocephaly
  • Marfan Syndrome
  • Maroteaux Lamy Syndrome
  • Maturity Onset Diabetes Of The Young
  • Max Gene
  • Mckusick-Kaufman Syndrome (Mkks)
  • Met Gene
  • Met Proto-Oncogene Receptor Tyrosine Kinase Mutation
  • Metabolic Acidosis
  • Metabolic Disorders (Inherited)
  • Microcephaly
  • Micrognathia
  • Microphthalmos
  • Mitf Gene
  • Mitochondrial Disorders
  • Mlh1 Gene
  • Morquio Brailsford Syndrome
  • Mre11a Gene
  • Msh2 Gene
  • Msh3 Gene
  • Msh6 Gene
  • Mthfr Mutation
  • Mucklewells Syndrome
  • Mucopolysaccharidosis
  • Multifactorial Inheritance
  • Multiple Congenital Anomalies And Birth Defects
  • Multiple Epiphyseal Dysplasia
  • Muscular Dystrophy
  • Mutyh Gene
  • Myoclonic Epilepsy With Ragged Red Fibers
  • Myotonic Dystrophy
  • Nbn Gene
  • Neonatal Adrenoleukodystrophy
  • Neural Tube Defects
  • Neurofibromatosis
  • Neuronal Migration Disorders
  • Neuropathy
  • Neurotransmitter Abnormalities
  • Neutrophil Disorders
  • Niemann Pick Disease
  • Noonan Syndrome
  • Nthl1 Gene
  • Ntric Fusion Mutation
  • Nudt15 Mutation
  • Nystagmus
  • Obesity
  • Opsoclonus Myoclonus Ataxia Syndrome
  • Osteogenesis Imperfecta
  • Osteopetrosis
  • Osteoporosis
  • Paramyotonia Congenita
  • Pdgfra Gene
  • Pediatric Cancer
  • Peroxisomal Disorders
  • Peutz Jeghers Syndrome
  • Phenylketonuria
  • Pierre Robin Sequence
  • Plagiocephaly
  • Pms2 Gene
  • Poland Syndrome
  • Pold1 Gene
  • Pole Gene
  • Polycystic Kidney Disease
  • Polydactyly Hand
  • Porphyria
  • Port Wine Stain
  • Prader Willi Syndrome
  • Precision Medicine
  • Preconception Counseling
  • Prenatal Genetic Counseling
  • Prenatal Testing
  • Preventive Medicine
  • Proto-Oncogene B-Raf And V-Raf Murine Sarcoma Viral Oncogene Homolog B Mutation
  • Ptch1 Gene
  • Rad50 Gene
  • Rad51c Gene
  • San Filippo Syndrome
  • Scn1a Related Seizures Disorders
  • Scn2a Mutation
  • Sdha Gene
  • Sdhaf2 Gene
  • Sdhb Gene
  • Sdhc Gene
  • Sdhd Gene
  • Short Stature
  • Shwachman Diamond Syndrome
  • Slos Smith Lemli Opitz Syndrome
  • Smad4 Gene
  • Smarca4 Gene
  • Smarcb1 Gene
  • Smith-Magenis Syndrome
  • Speech Delay
  • Spinal Muscular Atrophy
  • Splenomegaly
  • Spondylo-Meta-Epiphyseal Dysplasia
  • Stickler Syndrome
  • Sufu Gene
  • Syndactyly
  • Tay Sachs Disease
  • Thumb Hypoplasia
  • Tmem127 Gene
  • Tpmt Mutation
  • Trisomy 13
  • Tuberous Sclerosis
  • Turner Syndrome
  • Twin Types
  • Tyrosinemia
  • Ventriculomegaly
  • Vhl Gene
  • Virtual Care
  • Williams Syndrome
  • Wilms Tumor 1 Mutations
  • Wilson's Disease