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KCNQ1OT1
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51
disease terms (MeSH) has been reported with KCNQ1OT1 gene.
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[Click  to re-sort the table]
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Meta-analysis Publications
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Beckwith-Wiedemann Syndrome
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15
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0
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Silver-Russell Syndrome
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6
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0
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Infertility, Male
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4
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0
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Infertility
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4
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0
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Uniparental Disomy
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4
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0
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Liver Neoplasms
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3
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0
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Neoplasms
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3
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0
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Wilms Tumor
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3
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0
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Fetal Growth Retardation
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2
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0
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Colorectal Neoplasms
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2
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0
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Growth Disorders
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2
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0
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Placenta Diseases
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2
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0
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Hernia, Umbilical
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2
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0
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Genetic Diseases, Inborn
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2
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0
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Long QT Syndrome
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2
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0
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Overweight
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1
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0
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Adenocarcinoma, Papillary
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1
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0
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Heart Defects, Congenital
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1
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0
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Hypertrophy
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1
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0
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Abnormalities, Multiple
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1
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0
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Death, Sudden, Cardiac
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1
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0
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Disease Progression
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1
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0
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Fetal Diseases
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1
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0
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Fetal Macrosomia
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1
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0
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Monosomy
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1
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0
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Syncope
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1
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0
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Uterine Neoplasms
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1
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0
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Hypocalcemia
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1
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0
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Infant, Newborn, Diseases
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1
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0
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Carcinoma, Pancreatic Ductal
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1
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0
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Diabetes Mellitus, Type 2
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1
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0
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Pseudohypoparathyroidism
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1
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0
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Diseases in Twins
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1
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0
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Heart Arrest
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1
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0
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Syndrome
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1
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0
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Genomic Instability
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1
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0
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Adenocarcinoma, Mucinous
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1
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0
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Birth Weight
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1
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0
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Hepatoblastoma
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1
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0
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Infertility, Female
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1
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0
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Kidney Neoplasms
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1
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0
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Pancreatic Neoplasms
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1
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0
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Chromosome Aberrations
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1
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0
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Diabetes Mellitus
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1
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0
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Oligospermia
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1
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0
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Developmental Disabilities
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1
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0
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Hypoglycemia
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1
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0
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Klippel-Trenaunay-Weber Syndrome
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1
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0
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Hydatidiform Mole
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1
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0
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Hyperphosphatemia
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1
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0
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Abortion, Spontaneous
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1
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0
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Note: The number of publications displayed in this table will differ from the number displayed in the HuGE Literature Finder as the number
in Genopedia reflects only the indexed disease term without children terms, but the number in the HuGE Literature Finder
reflects all text searches of the disease term including the indexed term and corresponding children terms.
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