MeSH Treeview
Query OMIM entry list
600289
MAPK14
MITOGEN-ACTIVATED PROTEIN KINASE 14
→
High-scoring List
Neoplasms
Hamartoma
Tuberous Sclerosis
Neoplasms by Histologic Type
Leukemia
Leukemia, Myeloid
Leukemia, Myeloid, Acute
Leukemia, Erythroblastic, Acute
Neoplasms by Site
Digestive System Neoplasms
Liver Neoplasms
Liver Neoplasms, Experimental
Neoplasms, Experimental
Liver Neoplasms, Experimental
Neoplasms, Multiple Primary
Tuberous Sclerosis
Neoplastic Syndromes, Hereditary
Tuberous Sclerosis
Digestive System Diseases
Digestive System Neoplasms
Liver Neoplasms
Liver Neoplasms, Experimental
Gastrointestinal Diseases
Gastroenteritis
Colitis
Colitis, Ulcerative
Inflammatory Bowel Diseases
Colitis, Ulcerative
Crohn Disease
Intestinal Diseases
Colonic Diseases
Colitis
Colitis, Ulcerative
Inflammatory Bowel Diseases
Colitis, Ulcerative
Crohn Disease
Liver Diseases
Liver Neoplasms
Liver Neoplasms, Experimental
Nervous System Diseases
Central Nervous System Diseases
Spinal Cord Diseases
Amyotrophic Lateral Sclerosis
Nervous System Malformations
Malformations of Cortical Development
Tuberous Sclerosis
Neurocutaneous Syndromes
Tuberous Sclerosis
Neurodegenerative Diseases
Heredodegenerative Disorders, Nervous System
Tuberous Sclerosis
Motor Neuron Disease
Amyotrophic Lateral Sclerosis
TDP-43 Proteinopathies
Amyotrophic Lateral Sclerosis
Neuromuscular Diseases
Motor Neuron Disease
Amyotrophic Lateral Sclerosis
Peripheral Nervous System Diseases
Neuritis
Radiculopathy
Cardiovascular Diseases
Heart Diseases
Cardiomyopathies
Cardiomyopathy, Restrictive
Myocardial Ischemia
Coronary Disease
Vascular Diseases
Arterial Occlusive Diseases
Arteriosclerosis
Atherosclerosis
Embolism and Thrombosis
Thrombosis
Myocardial Ischemia
Coronary Disease
Hemic and Lymphatic Diseases
Hematologic Diseases
Anemia
Bone Marrow Diseases
Myeloproliferative Disorders
Leukemia, Erythroblastic, Acute
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormalities
Nervous System Malformations
Malformations of Cortical Development
Tuberous Sclerosis
Genetic Diseases, Inborn
Heredodegenerative Disorders, Nervous System
Tuberous Sclerosis
Neoplastic Syndromes, Hereditary
Tuberous Sclerosis
Skin and Connective Tissue Diseases
Skin Diseases
Skin Diseases, Vesiculobullous
Pemphigus
Nutritional and Metabolic Diseases
Metabolic Diseases
Proteostasis Deficiencies
TDP-43 Proteinopathies
Amyotrophic Lateral Sclerosis
Immune System Diseases
Autoimmune Diseases
Pemphigus
Animal Diseases
Disease Models, Animal
Pathological Conditions, Signs and Symptoms
Pathologic Processes
Disease Attributes
Acute Disease
Chronic Disease
Inflammation
Necrosis
Database Center for Life Science