Overview
Jung Ko practices practicing medicine in Seoul, Republic of Korea.
Ko is highly rated in 38 conditions, according to our data. Their clinical expertise encompasses Kabuki Syndrome, Hemihyperplasia, Sotos Syndrome, Osteotomy, and Small Bowel Resection.
They are actively involved in clinical research, co-authoring 153 peer reviewed articles.
Locations
Clinical Research
Clinical research consists of overseeing clinical studies of patients undergoing new treatments and therapies, and publishing articles in peer reviewed medical journals. Experts who actively participate in clinical research are generally at the forefront of the fields and aware of the most up-to-date advances in treatments for their patients.
Frequently Asked Questions about Jung M. Ko
Is Jung M. Ko a top-rated expert for Kabuki Syndrome?
MediFind is an objective health platform that identifies experts based on real-world data. Jung M. Ko is classified as an Distinguished expert for Kabuki Syndrome, meaning they are among the top experts in the country for this condition. This ranking is based on their volume of patients, published research, and peer connections.
Does Jung M. Ko participate in research or clinical trials?
Yes. Jung M. Ko has published 153 articles and abstracts on conditions like Kabuki Syndrome. You can view a list of Jung M. Ko's latest peer-reviewed publications and clinical trial participation on their profile to see if they are active in new treatments.
Areas of Expertise
MediFind evaluates expertise by pulling from factors such as number of articles a doctor has published in medical journals, participation in clinical trials, speaking at industry conferences, prescribing and referral patterns, and strength of connections with other experts in their field.
Learn more about MediFind’s expert tiers
- Distinguished
- Kabuki SyndromeKo isDistinguished. Learn about Kabuki Syndrome.
- Advanced
- Acanthosis Nigricans
- AchondroplasiaKo isAdvanced. Learn about Achondroplasia.
- Acromicric Dysplasia
- Aplasia Cutis Congenita
- Beckwith-Wiedemann Syndrome
- Brachydactyly Mononen Type
- Cardiofaciocutaneous Syndrome
- ChondrodystrophyKo isAdvanced. Learn about Chondrodystrophy.
- Chromosome 6 Uniparental Disomy
- Clouston SyndromeKo isAdvanced. Learn about Clouston Syndrome.
- Ectodermal Dysplasias
- GigantismKo isAdvanced. Learn about Gigantism.
- Glutaric Acidemia Type 2
- Hemi 3 SyndromeKo isAdvanced. Learn about Hemi 3 Syndrome.
- HemihyperplasiaKo isAdvanced. Learn about Hemihyperplasia.
- Hennekam SyndromeKo isAdvanced. Learn about Hennekam Syndrome.
- Hereditary Mucoepithelial Dysplasia
- Holocarboxylase Synthetase Deficiency
- HypochondroplasiaKo isAdvanced. Learn about Hypochondroplasia.
- Kyphomelic Dysplasia
- Lysinuric Protein Intolerance
- MacroglossiaKo isAdvanced. Learn about Macroglossia.
- Malonyl-CoA Decarboxylase Deficiency
- MosaicismKo isAdvanced. Learn about Mosaicism.
- Muenke SyndromeKo isAdvanced. Learn about Muenke Syndrome.
- Ornithine Transcarbamylase Deficiency
- Penis AgenesisKo isAdvanced. Learn about Penis Agenesis.
- RASopathiesKo isAdvanced. Learn about RASopathies.
- Rubinstein-Taybi Syndrome
- Russell-Silver Dwarfism
- Schwartz-Jampel Syndrome
- Shwachman-Diamond Syndrome
- Sotos SyndromeKo isAdvanced. Learn about Sotos Syndrome.
- Umbilical HerniaKo isAdvanced. Learn about Umbilical Hernia.
- Urea Cycle Disorders (UCD)
- VisceromegalyKo isAdvanced. Learn about Visceromegaly.
- X-Linked Spondyloepiphyseal Dysplasia Tarda
- Experienced
- Achalasia Microcephaly Syndrome
- AcrocephalopolydactylyKo isExperienced. Learn about Acrocephalopolydactyly.
- Acrofacial Dysostosis Rodriguez Type
- Acrofrontofacionasal Dysostosis Syndrome
- Adrenal Insufficiency Pediatric
- AlbinismKo isExperienced. Learn about Albinism.
- Albright's Hereditary Osteodystrophy
- Anti-NMDA Receptor Encephalitis
- Apert SyndromeKo isExperienced. Learn about Apert Syndrome.
- Apolipoprotein C2 Deficiency
- Argininosuccinic Aciduria
- Arthrogryposis Multiplex Congenita
- Bartter SyndromeKo isExperienced. Learn about Bartter Syndrome.
- Bile Duct ObstructionKo isExperienced. Learn about Bile Duct Obstruction.
- BrachydactylyKo isExperienced. Learn about Brachydactyly.
- CardiomyopathyKo isExperienced. Learn about Cardiomyopathy.
- Central Sleep ApneaKo isExperienced. Learn about Central Sleep Apnea.
- CHARGE SyndromeKo isExperienced. Learn about CHARGE Syndrome.
- Childhood PancreatitisKo isExperienced. Learn about Childhood Pancreatitis.
- CholestasisKo isExperienced. Learn about Cholestasis.
- Cholesteryl Ester Storage Disease
- CitrullinemiaKo isExperienced. Learn about Citrullinemia.
- Congenital Central Hypoventilation Syndrome
- Congenital ContracturesKo isExperienced. Learn about Congenital Contractures.
- Congenital Hyperinsulinism
- Congenital Nephrotic Syndrome
- Congenital Radioulnar Synostosis
- Cortical DysplasiaKo isExperienced. Learn about Cortical Dysplasia.
- Costello SyndromeKo isExperienced. Learn about Costello Syndrome.
- Craniofrontonasal Dysplasia
- CraniosynostosisKo isExperienced. Learn about Craniosynostosis.
- Crouzon SyndromeKo isExperienced. Learn about Crouzon Syndrome.
- Cystic FibrosisKo isExperienced. Learn about Cystic Fibrosis.
- Delayed GrowthKo isExperienced. Learn about Delayed Growth.
- Down SyndromeKo isExperienced. Learn about Down Syndrome.
- Dyskeratosis CongenitaKo isExperienced. Learn about Dyskeratosis Congenita.
- Enlarged LiverKo isExperienced. Learn about Enlarged Liver.
- Epidermolysis BullosaKo isExperienced. Learn about Epidermolysis Bullosa.
- Familial Hypertriglyceridemia
- Familial Lipoprotein Lipase Deficiency
- Farber Lipogranulomatosis
- Fibrolamellar CarcinomaKo isExperienced. Learn about Fibrolamellar Carcinoma.
- GangliosidosisKo isExperienced. Learn about Gangliosidosis.
- Gaucher DiseaseKo isExperienced. Learn about Gaucher Disease.
- Gaucher Disease Type 1Ko isExperienced. Learn about Gaucher Disease Type 1.
- Genital DwarfismKo isExperienced. Learn about Genital Dwarfism.
- Griscelli SyndromeKo isExperienced. Learn about Griscelli Syndrome.
- Hearing LossKo isExperienced. Learn about Hearing Loss.
- Hereditary KeratitisKo isExperienced. Learn about Hereditary Keratitis.
- Herpes Simplex Encephalitis
- HydrocephalusKo isExperienced. Learn about Hydrocephalus.
- Hydrocephalus due to Congenital Stenosis of Aqueduct of Sylvius
- Hydrocephalus Skeletal Anomalies
- HyperaldosteronismKo isExperienced. Learn about Hyperaldosteronism.
- Hypertrophic Cardiomyopathy (HCM)
- Hypohidrotic Ectodermal Dysplasia
- HypophosphatemiaKo isExperienced. Learn about Hypophosphatemia.
- HypopituitarismKo isExperienced. Learn about Hypopituitarism.
- Incontinentia PigmentiKo isExperienced. Learn about Incontinentia Pigmenti.
- Increased Head Circumference
- IntersexKo isExperienced. Learn about Intersex.
- Kearns-Sayre SyndromeKo isExperienced. Learn about Kearns-Sayre Syndrome.
- KeloidsKo isExperienced. Learn about Keloids.
- Knock KneesKo isExperienced. Learn about Knock Knees.
- KyphosisKo isExperienced. Learn about Kyphosis.
- Lactic AcidosisKo isExperienced. Learn about Lactic Acidosis.
- Linear Nevus Sebaceous Syndrome
- Low Sodium LevelKo isExperienced. Learn about Low Sodium Level.
- LymphangiectasisKo isExperienced. Learn about Lymphangiectasis.
- Lysosomal Acid Lipase Deficiency
- MalnutritionKo isExperienced. Learn about Malnutrition.
- Maternal Hyperphenylalaninemia
- Metabolic AcidosisKo isExperienced. Learn about Metabolic Acidosis.
- Metopic RidgeKo isExperienced. Learn about Metopic Ridge.
- MicrocephalyKo isExperienced. Learn about Microcephaly.
- Microcephaly Deafness Syndrome
- MicrognathiaKo isExperienced. Learn about Micrognathia.
- Mucopolysaccharidoses (MPS)
- Mucopolysaccharidosis Type 2 (MPS II, Hunter Syndrome)
- Mucopolysaccharidosis Type 4 (MPS IV, Morquio Syndrome)
- Multiple Carboxylase Deficiency
- Myhre SyndromeKo isExperienced. Learn about Myhre Syndrome.
- Nail-Patella SyndromeKo isExperienced. Learn about Nail-Patella Syndrome.
- Nevoid Basal Cell Carcinoma Syndrome
- Noonan SyndromeKo isExperienced. Learn about Noonan Syndrome.
- OmphaloceleKo isExperienced. Learn about Omphalocele.
- Osteogenesis ImperfectaKo isExperienced. Learn about Osteogenesis Imperfecta.
- OsteotomyKo isExperienced. Learn about Osteotomy.
- Pachyonychia CongenitaKo isExperienced. Learn about Pachyonychia Congenita.
- PanhypopituitarismKo isExperienced. Learn about Panhypopituitarism.
- Pfeiffer SyndromeKo isExperienced. Learn about Pfeiffer Syndrome.
- PiebaldismKo isExperienced. Learn about Piebaldism.
- PIK3CA-Related Overgrowth Spectrum
- PlagiocephalyKo isExperienced. Learn about Plagiocephaly.
- PolymicrogyriaKo isExperienced. Learn about Polymicrogyria.
- Prader-Willi SyndromeKo isExperienced. Learn about Prader-Willi Syndrome.
- ProgeriaKo isExperienced. Learn about Progeria.
- Progressive External Ophthalmoplegia
- Progressive Osseous Heteroplasia
- Propionic AcidemiaKo isExperienced. Learn about Propionic Acidemia.
- Pseudohypoparathyroidism
- Pulmonary Valve Stenosis
- Pyle DiseaseKo isExperienced. Learn about Pyle Disease.
- RicketsKo isExperienced. Learn about Rickets.
- Saethre-Chotzen Syndrome
- Short-Chain Acyl-CoA Dehydrogenase Deficiency
- Small Bowel ResectionKo isExperienced. Learn about Small Bowel Resection.
- Spondyloepimetaphyseal Dysplasia Joint Laxity
- SyndactylyKo isExperienced. Learn about Syndactyly.
- Tay-Sachs DiseaseKo isExperienced. Learn about Tay-Sachs Disease.
- Thanatophoric DysplasiaKo isExperienced. Learn about Thanatophoric Dysplasia.
- Tracheoesophageal Fistula
- Treacher Collins Syndrome
- Trichorrhexis NodosaKo isExperienced. Learn about Trichorrhexis Nodosa.
- Undescended TesticleKo isExperienced. Learn about Undescended Testicle.
- Von Gierke DiseaseKo isExperienced. Learn about Von Gierke Disease.
- Wolman DiseaseKo isExperienced. Learn about Wolman Disease.
- X-Linked Hypophosphatemia
- Xeroderma PigmentosumKo isExperienced. Learn about Xeroderma Pigmentosum.