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Query OMIM entry list
212065
CDG1A
CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ia
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Neoplasms
Neoplasms by Histologic Type
Neoplasms, Connective and Soft Tissue
Neoplasms, Connective Tissue
Neoplasms, Bone Tissue
Osteochondroma
Osteochondromatosis
Exostoses, Multiple Hereditary
Neoplastic Syndromes, Hereditary
Exostoses, Multiple Hereditary
Musculoskeletal Diseases
Bone Diseases
Bone Diseases, Developmental
Osteochondrodysplasias
Osteochondroma
Osteochondromatosis
Exostoses, Multiple Hereditary
Hyperostosis
Exostoses
Exostoses, Multiple Hereditary
Digestive System Diseases
Liver Diseases
Liver Cirrhosis
Nervous System Diseases
Central Nervous System Diseases
Brain Diseases
Basal Ganglia Diseases
Multiple System Atrophy
Olivopontocerebellar Atrophies
Cerebellar Diseases
Dandy-Walker Syndrome
Spinocerebellar Degenerations
Olivopontocerebellar Atrophies
Hydrocephalus
Dandy-Walker Syndrome
Intracranial Hypertension
Hydrocephalus
Dandy-Walker Syndrome
Movement Disorders
Multiple System Atrophy
Olivopontocerebellar Atrophies
Spinal Cord Diseases
Spinocerebellar Degenerations
Olivopontocerebellar Atrophies
Cranial Nerve Diseases
Ocular Motility Disorders
Strabismus
Esotropia
Demyelinating Diseases
Nervous System Malformations
Dandy-Walker Syndrome
Neurodegenerative Diseases
Heredodegenerative Disorders, Nervous System
Spinocerebellar Degenerations
Olivopontocerebellar Atrophies
Multiple System Atrophy
Olivopontocerebellar Atrophies
Olivopontocerebellar Atrophies
Neurologic Manifestations
Neurobehavioral Manifestations
Intellectual Disability
Psychomotor Disorders
Sensation Disorders
Vision Disorders
Neuromuscular Diseases
Eye Diseases
Eye Diseases, Hereditary
Retinitis Pigmentosa
Ocular Motility Disorders
Strabismus
Esotropia
Retinal Diseases
Retinal Degeneration
Retinal Dystrophies
Retinitis Pigmentosa
Vision Disorders
Male Urogenital Diseases
Urologic Diseases
Kidney Diseases
Kidney Diseases, Cystic
Nephrosis
Nephrotic Syndrome
Female Urogenital Diseases and Pregnancy Complications
Female Urogenital Diseases
Urologic Diseases
Kidney Diseases
Kidney Diseases, Cystic
Nephrosis
Nephrotic Syndrome
Pregnancy Complications
Fetal Diseases
Erythroblastosis, Fetal
Hydrops Fetalis
Cardiovascular Diseases
Cardiovascular Abnormalities
Heart Defects, Congenital
Heart Diseases
Cardiomegaly
Cardiomyopathies
Cardiomyopathy, Hypertrophic
Heart Defects, Congenital
Heart Valve Diseases
Aortic Valve Stenosis
Aortic Stenosis, Subvalvular
Cardiomyopathy, Hypertrophic
Pericardial Effusion
Hemic and Lymphatic Diseases
Hematologic Diseases
Anemia
Anemia, Hemolytic
Anemia, Hemolytic, Congenital
Anemia, Dyserythropoietic, Congenital
Blood Coagulation Disorders
Blood Coagulation Disorders, Inherited
Antithrombin III Deficiency
Factor XI Deficiency
Protein C Deficiency
Coagulation Protein Disorders
Factor XI Deficiency
Protein S Deficiency
Blood Group Incompatibility
Erythroblastosis, Fetal
Hydrops Fetalis
Blood Platelet Disorders
Thrombocytopenia
Blood Protein Disorders
Antithrombin III Deficiency
Hypoproteinemia
Hypoalbuminemia
Protein C Deficiency
Protein S Deficiency
Hemoglobinopathies
Thalassemia
alpha-Thalassemia
Hydrops Fetalis
Hemorrhagic Disorders
Factor XI Deficiency
Thrombophilia
Antithrombin III Deficiency
Protein C Deficiency
Protein S Deficiency
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormalities
Abnormalities, Multiple
Cardiovascular Abnormalities
Heart Defects, Congenital
Chromosome Disorders
Nervous System Malformations
Dandy-Walker Syndrome
Fetal Diseases
Erythroblastosis, Fetal
Hydrops Fetalis
Genetic Diseases, Inborn
Anemia, Hemolytic, Congenital
Anemia, Dyserythropoietic, Congenital
Blood Coagulation Disorders, Inherited
Antithrombin III Deficiency
Factor XI Deficiency
Protein C Deficiency
Chromosome Disorders
Eye Diseases, Hereditary
Retinitis Pigmentosa
Hemoglobinopathies
Thalassemia
alpha-Thalassemia
Hydrops Fetalis
Heredodegenerative Disorders, Nervous System
Spinocerebellar Degenerations
Olivopontocerebellar Atrophies
Metabolism, Inborn Errors
Carbohydrate Metabolism, Inborn Errors
Congenital Disorders of Glycosylation
Lipid Metabolism, Inborn Errors
Hypolipoproteinemias
Progeria
Neoplastic Syndromes, Hereditary
Exostoses, Multiple Hereditary
Nutritional and Metabolic Diseases
Metabolic Diseases
Glucose Metabolism Disorders
Hyperinsulinism
Hypoglycemia
Lipid Metabolism Disorders
Dyslipidemias
Hyperlipidemias
Hyperlipoproteinemias
Hypolipoproteinemias
Metabolism, Inborn Errors
Carbohydrate Metabolism, Inborn Errors
Congenital Disorders of Glycosylation
Lipid Metabolism, Inborn Errors
Hypolipoproteinemias
Progeria
Immune System Diseases
Blood Group Incompatibility
Erythroblastosis, Fetal
Hydrops Fetalis
Pathological Conditions, Signs and Symptoms
Pathological Conditions, Anatomical
Atrophy
Hypertrophy
Cardiomegaly
Pathologic Processes
Chromosome Aberrations
Disease
Syndrome
Disease Attributes
Disease Susceptibility
Genetic Predisposition to Disease
Diseases in Twins
Recurrence
Growth Disorders
Signs and Symptoms
Body Weight
Edema
Hydrops Fetalis
Failure to Thrive
Neurologic Manifestations
Neurobehavioral Manifestations
Intellectual Disability
Psychomotor Disorders
Sensation Disorders
Vision Disorders
Substance-Related Disorders
Alcohol-Related Disorders
Alcoholic Intoxication
Alcoholism
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