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Query OMIM entry list
182860
SPTA1
SPECTRIN, ALPHA, ERYTHROCYTIC 1
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Neoplasms
Neoplasms by Histologic Type
Leukemia
Leukemia, Lymphoid
Leukemia, T-Cell
Neoplasms by Site
Digestive System Neoplasms
Gastrointestinal Neoplasms
Intestinal Neoplasms
Colorectal Neoplasms
Colonic Neoplasms
Digestive System Diseases
Digestive System Neoplasms
Gastrointestinal Neoplasms
Intestinal Neoplasms
Colorectal Neoplasms
Colonic Neoplasms
Gastrointestinal Diseases
Gastrointestinal Neoplasms
Intestinal Neoplasms
Colorectal Neoplasms
Colonic Neoplasms
Intestinal Diseases
Colonic Diseases
Colorectal Neoplasms
Colonic Neoplasms
Intestinal Neoplasms
Colorectal Neoplasms
Colonic Neoplasms
Nervous System Diseases
Central Nervous System Diseases
Brain Diseases
Brain Diseases, Metabolic
Brain Diseases, Metabolic, Inborn
Phenylketonurias
Spinal Cord Diseases
Muscular Atrophy, Spinal
Nervous System Malformations
Hereditary Sensory and Motor Neuropathy
Charcot-Marie-Tooth Disease
Neurodegenerative Diseases
Heredodegenerative Disorders, Nervous System
Hereditary Sensory and Motor Neuropathy
Charcot-Marie-Tooth Disease
Motor Neuron Disease
Muscular Atrophy, Spinal
Neuromuscular Diseases
Motor Neuron Disease
Muscular Atrophy, Spinal
Muscular Atrophy, Spinal
Peripheral Nervous System Diseases
Polyneuropathies
Hereditary Sensory and Motor Neuropathy
Charcot-Marie-Tooth Disease
Hemic and Lymphatic Diseases
Hematologic Diseases
Anemia
Anemia, Hemolytic
Anemia, Hemolytic, Congenital
Elliptocytosis, Hereditary
Spherocytosis, Hereditary
Lymphatic Diseases
Lymphoproliferative Disorders
Leukemia, Lymphoid
Leukemia, T-Cell
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormalities
Nervous System Malformations
Hereditary Sensory and Motor Neuropathy
Charcot-Marie-Tooth Disease
Genetic Diseases, Inborn
Anemia, Hemolytic, Congenital
Elliptocytosis, Hereditary
Spherocytosis, Hereditary
Heredodegenerative Disorders, Nervous System
Hereditary Sensory and Motor Neuropathy
Charcot-Marie-Tooth Disease
Metabolism, Inborn Errors
Amino Acid Metabolism, Inborn Errors
Phenylketonurias
Brain Diseases, Metabolic, Inborn
Phenylketonurias
Nutritional and Metabolic Diseases
Metabolic Diseases
Brain Diseases, Metabolic
Brain Diseases, Metabolic, Inborn
Phenylketonurias
Metabolism, Inborn Errors
Amino Acid Metabolism, Inborn Errors
Phenylketonurias
Brain Diseases, Metabolic, Inborn
Phenylketonurias
Immune System Diseases
Immunoproliferative Disorders
Lymphoproliferative Disorders
Leukemia, Lymphoid
Leukemia, T-Cell
Pathological Conditions, Signs and Symptoms
Pathologic Processes
Chromosome Aberrations
Hyperbilirubinemia
Jaundice
Signs and Symptoms
Skin Manifestations
Jaundice
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