Photo of Grace J. Noh, MD

Grace J. Noh, MD

Medical Genetics
Accepting New Patients
Providence Clinical Genetics and Genomics Program - Burbank
181 South Buena Vista Street, Suite 110
Burbank, CA 91505
16.0 miles away
(818) 748-4748
Medical Groups & Affiliations
Providence Medical Institute
Speaks: English
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Providence Clinical Genetics and Genomics Program - Burbank

181 South Buena Vista Street, Suite 110, Burbank, CA 91505

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Insurances Accepted

This information provides an overview of accepted insurance plan types. Coverage may vary by specific plan. Please verify your with your insurance provider before visiting us for care.

About Grace J. Noh

Dr. Grace Noh is a medical geneticist practicing with The Roy and Patricia Disney Family Cancer Center in Burbank, CA. She believes in open and honest communications lines with her patients while prioritizing compassionate care to foster positive health outcomes.

Board Certifications
  • American Board of Internal Medicine, Internal Medicine
  • American Board of Medical Genetics and Genomics, Clinical Genetics (MD)
Providence Clinical Genetics and Genomics Program - Burbank
181 South Buena Vista Street, Suite 110
Burbank, CA 91505
Medical Groups & Affiliations
Providence Medical Institute

Conditions and Procedures

  • 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
  • Alstrom Syndrome
  • Anal Stenosis
  • Androgen Insensitivity
  • Aneuploidy
  • 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
  • Blm Heterozygotes
  • 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
  • Cdh1 Gene Mutation
  • 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
  • Coffin-Lowry Syndrome
  • Coloboma
  • Congenital Adrenal Hyperplasia
  • Congenital Deformities
  • 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
  • Ctnna1 Gene Mutation
  • Cutis Aplasia
  • Cyp2c19 Mutation
  • Cyp2d6 Mutation
  • Cystic Fibrosis
  • Cystic Fibrosis Gene Carrier
  • Cystic Fibrosis Genetic Testing
  • 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
  • Emanuel Syndrome
  • Epcam Gene
  • Epilepsy
  • Esophageal Atresia
  • Exercise Intolerance
  • Facial Asymmetry
  • Facioscapulohumeral Muscular Dystrophy
  • Failure To Thrive
  • Familial Dysautonomia
  • Familial Hemiplegic Migraine
  • 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 Chromosomal Abnormalities
  • Fetal Growth Restriction
  • Fh Tumor Predisposition Syndrome
  • Fish Cancer Test
  • Flcn Gene
  • Fracture
  • Fragile X Syndrome
  • Frasier Syndrome
  • Fumarate Hydratase Deficiency
  • Galnt12 Gene
  • Gaucher Disease
  • Genetic Causes Of Vascular Malformations
  • Genetic Cervical Spine Conditions
  • Genetic Counseling
  • Genetic Disorders
  • Genetic Dystonia
  • Genetic Leukoencephalopathy
  • Genetic Testing Colon Cancer
  • Genetic Testing Ovarian Cancer
  • Glass Syndrome
  • 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
  • Hepatomegaly
  • 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
  • Hypochondroplasia
  • Hypoglycemia
  • Hypohidrotic Ectodermal Dysplasia
  • Hypophosphatasia
  • Hypospadias
  • Hypotonia
  • I1307k Gene Mutation
  • Immune Deficiency
  • Inborn Errors Of Metabolism
  • Infertility
  • Intellectual Disabilities
  • Intestinal Atresia
  • Ipex Syndrome
  • Jacob's Syndrome
  • Joint Hypermobility Syndrome
  • Kabuki Syndrome
  • Kcnb1 Mutation
  • Kcnc1-Related Disorders
  • Kcnq2-Related Epilepsies
  • Kearns Sayre Syndrome
  • Kidney Dysplasia
  • Kit Gene
  • Klinefelter Syndrome
  • Klippel Trenaunay Syndrome
  • L1 Syndrome
  • Learning Disabilities
  • Learning Disorders
  • Leber Congenital Amaurosis
  • Leber Hereditary Optic Neuropathy
  • Legius Syndrome
  • Leigh's Disease
  • Leukodystrophy
  • Li Fraumeni Syndrome
  • Lissencephaly
  • Long Qt Syndrome
  • Lynch Syndrome
  • Lysosomal Diseases
  • Macrocephaly
  • Malignant Hyperthermia
  • Malignant Hyperthermia Susceptibility
  • 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
  • Met Translocation
  • Metabolic Acidosis
  • Metabolic Disorders (Inherited)
  • Microcephaly
  • Micrognathia
  • Microphthalmos
  • Mitf Gene
  • Mitochondrial Disorders
  • Mlh1 Gene
  • Morquio Brailsford Syndrome
  • Mre11a Gene
  • Msh2 Gene
  • Msh3 Biallelic Pathogenic Variants
  • Msh3 Gene
  • Msh6 Gene
  • Mthfr Mutation
  • Mucklewells Syndrome
  • Mucopolysaccharidosis
  • Multifactorial Inheritance
  • Multiple Congenital Anomalies And Birth Defects
  • Multiple Epiphyseal Dysplasia
  • Muscular Dystrophy
  • Mutyh Biallelic Pathogenic Variants
  • Mutyh Gene
  • Mutyh Heterozygotes
  • Myoclonic Epilepsy With Ragged Red Fibers
  • Myotonic Dystrophy
  • Nbn Gene
  • Neonatal Adrenoleukodystrophy
  • Neural Tube Defects
  • Neurofibromatosis
  • Neurogenetics
  • 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
  • Oral-Facial-Digital Syndrome
  • Osteogenesis Imperfecta
  • Osteopetrosis
  • Osteoporosis
  • Pallister-Killian Syndrome
  • Paramyotonia Congenita
  • Pcdh19-Epilepsy
  • Pdgfra Gene
  • Pediatric Cancer
  • Pendred Syndrome
  • 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
  • Prothrombin-Related Thrombophilia
  • Proto-Oncogene B-Raf And V-Raf Murine Sarcoma Viral Oncogene Homolog B Mutation
  • Ptch1 Gene
  • Rad50 Gene
  • Rad51c Gene
  • Ret Translocation
  • Robinow Syndrome
  • San Filippo Syndrome
  • Scn1a Related Seizures Disorders
  • Scn2a Mutation
  • Scn8a-Related Epilepsy
  • Sdha Gene
  • Sdhaf2 Gene
  • Sdhb Gene
  • Sdhc Gene
  • Sdhd Gene
  • Sdhx Gene Mutation
  • Short Stature
  • Shwachman Diamond Syndrome
  • Slos Smith Lemli Opitz Syndrome
  • Smad4 Gene
  • Smarca4 Gene
  • Smarcb1 Gene
  • Smith-Magenis Syndrome
  • Sotos Syndrome
  • Speech Delay
  • Spinal Muscular Atrophy
  • Splenomegaly
  • Spondylo-Meta-Epiphyseal Dysplasia
  • Stickler Syndrome
  • Stkm11 Gene Mutation
  • Stxbp1-Related Disorders
  • Sufu Gene
  • Syndactyly
  • Tay Sachs Disease
  • Thumb Hypoplasia
  • Tmem127 Gene
  • Townes-Brocks Syndrome
  • Tpmt Mutation
  • Triple A Syndrome
  • Trisomy 13
  • Tuberous Sclerosis
  • Turner Syndrome
  • Twin Types
  • Tyrosinemia
  • Ventriculomegaly
  • Vhl Gene
  • Virtual Care
  • Waardenburg Syndrome
  • Whole Exome Sequencing
  • Whole Genome Sequencing
  • Williams Syndrome
  • Wilms Tumor 1 Mutations
  • Wilson's Disease
  • Xeroderma Pigmentosum
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